Texas Glutathione Lawsuit Attorney
If you got sick after a glutathione IV drip at a wellness clinic or an injection from affected vials shipped to your home, you may have a compounded glutathione lawsuit. The glutathione recalls are linked to endotoxin contamination that has caused severe infections, hospitalizations, and medical bills you shouldn’t have faced.
Compounded glutathione is mixed with other ingredients by a pharmacy, not manufactured as an FDA-approved injectable drug. Its dietary supplement grade label skips much of the testing that identifies contamination before reaching consumers. When quality control fails, the endotoxin goes straight into a person’s vein.
Injured patients can file glutathione lawsuits against more than one party. A defective product claim targets the supply chain: the supplier and pharmacy that compounded material never meant for injection. A malpractice claim targets the clinic, medspa, or provider who prescribed or injected glutathione without verifying the ingredient or warning you the drug was not FDA-approved.
We provide free consultations; you don’t pay unless we win.
Call 210-366-4949 to speak with a Texas glutathione injury lawyer today.
Product Defect & Medical Negligence
Janicek Law litigates both product defect and medical negligence claims. The most serious cases live where those two avenues converge.
Board-Certified Trial Attorney
More than 30 years taking on hospitals, physicians, and their insurers.
Board-Certified Trial Attorney
A longstanding record of success in complex drug and medical device litigation.
Patients and families across Texas benefit from the firm's knowledge, experience, and resources.
Check Your Product and Lot
This tool checks what you received against the lot numbers on the current FDA recall list. It does not assess your health or your legal options.
Was Contaminated Glutathione in Your IV Drip?
Compounded glutathione is rarely sold under its own product name. Common drip names include:
🌟 Aesthetic & Skin-Brightening Slang: common industry terms for skin brightening, hyperpigmentation, anti-aging, and other aesthetic treatments:
- Glow Drip
- Snow White Drip
- Cinderella Drip
- Melanin Blocker/Skin Whitening Drip
- Gluta Cocktail
💧 Wellness & Custom Add-On Slang: intravenous treatments marketed for anti-aging or detox after illness or stress:
- Deep Detox Drip
- The Fountain of Youth
🥂 Recovery & Hangover IV Therapies
- Hangover IV Therapy
- The Myers’ Cocktail (Upgraded)
The Safety Problem
Dietary supplement grade labels are not appropriate ingredients for compounding injectable products. Glutathione is not an FDA-approved drug by any stretch.
CDC & FDA Investigation: “Dietary Supplement Grade Label Is Not Appropriate Ingredient For Injectable Compounded Drugs”
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July 2026
Outbreak Begins
The Texas Department of State Health Services alerts the CDC after multiple patients suffered severe reactions to IV glutathione at an outpatient wellness clinic, prompting a multi-state CDC investigation.
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August 5, 2026
First Recall
Victory Medical Center Pharmacy issues a voluntary nationwide recall after testing identifies elevated endotoxin levels.
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August 19, 2026
Second Recall
Optimal Balance Pharmacy issues its voluntary nationwide recall for the same elevated bacterial endotoxin levels.
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August 20, 2026
Medisca Inc. Warns Pharmacies
Ingredient supplier Medisca Inc. tells pharmacies to stop using its dietary supplement-grade glutathione for sterile injectable drug compounding and notifies the FDA the same day.
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August 27, 2026
Contamination Source Identified & Second Warning to Pharmacists
Every recalled lot traced back to contamination in one lot: Lot Number 229536 from Medisca Inc. The FDA warns pharmacies again that the product was labeled dietary supplement grade and was not an appropriate ingredient for compounding glutathione injectable drugs. The agency's safety alert reports at least 30 adverse reactions, 3 hospitalizations, and 1 ICU admission for shock and abnormal blood clotting.
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September 9, 2026
Centric Compounding Recall
Centric Compounding conducted recalls related to their lots of compounded glutathione.
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September 13, 2026
FDA Publishes the Recall
The FDA publishes Centric Compounding's recall, adding an additional 9 direct adverse event reports from its distributed vials.
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September 16, 2026
CDC Investigation Update
The CDC publishes its formal investigation update, tracking 25 verified cases across Texas, Washington, Florida, and New York.
Harmed by a contaminated glutathione injection? Talk to our team about your legal options.
Glutathione Recall
Three Texas pharmacies have recalled lots of compounded glutathione tied to one lot of raw ingredient: Lot Number: 229536. The failure began upstream of every pharmacy involved, so this is not a handful of certain lots. It is a supply chain failure that can reach any pharmacy that ignored the agency’s labeling.
The recalled lots were sent to healthcare providers, med spas, or shipped directly to consumers for in-home injections. If you’ve been injured, you need Texas drug injury lawyers who handle recalled medication claims to investigate both avenues.
Victory Medical Center Pharmacy Recall (Austin)
Victory Medical Center Pharmacy issued the first of the three Texas recalls, after its own testing found elevated bacterial endotoxin. The injection site reactions in its adverse event reports point to intramuscular and subcutaneous injections, not IV alone.
| Recall Information | Details |
|---|---|
| Product | Compounded Glutathione 200 mg/mL, multi-dose vial |
| Recalled Lot Numbers | 1980571, 1981940, & 1984345 (all expire 8/27/2026) |
| Recall Date | 8/5/2026; Voluntary recall at the patient level |
| Recall Information | Victory Medical Center Pharmacy Recall |
| Distributed | Direct to consumers, clinics, & prescribers |
| States Affected | Florida, New York, & Texas |
| Number Of Adverse Events | Did not disclose |
| Reported Reactions | Severe headache, nausea, vomiting, fever, chills, tachycardia, blood pressure changes, injection site reactions, & body aches |
| Victory Medical Center Pharmacy Phone Number | 512-279-0985 |
Optimal Balance Pharmacy Recall (Houston)
Optimal Balance Pharmacy recalled one lot to the patient level, but that lot reached the widest distribution of the three recalled glutathione products.
| Recall Information | Details |
|---|---|
| Product | Compounded Glutathione 200 mg/mL, multi-dose vial |
| Recalled Lot Numbers | LG342009076 (expires 10/4/2026) |
| Recall Date | 8/19/2026; Voluntary recall at the patient level |
| Recall Information | Optimal Balance Pharmacy Recall |
| Distributed | Direct to consumers, clinics, & prescribers |
| States Affected | Arizona, Colorado, Florida, Illinois, Louisiana, Michigan, Nevada, New York, Oklahoma, Pennsylvania, Texas, Utah, Vermont, & Washington |
| Number Of Adverse Events | Did not disclose |
| Reported Reactions | Severe headache, nausea, vomiting, fever, chills, pain, and symptoms consistent with allergic/inflammatory reactions |
| Optimal Balance Pharmacy Phone Number | 281-919-2964 |
Centric Compounding Recall (Houston)
Centric Compounding recalled six lots across three product lines with elevated endotoxin levels distributed to healthcare providers and at the consumer level.
| Recall Information | Details |
|---|---|
| Product | Glutathione 200 mg/mL, Tri-Immune Boost & Myer’s Cocktail |
| Recalled Lot Numbers | Glutathione 200 mg/mL: 062326:B, 070826:A, & 072726:DTri-Immune Boost: 071626:BMyer’s Cocktail: 070226:D & 072126:A |
| Recall Date | FDA announced the Centric Compounding recall on 9/13/2026 at the consumer level |
| Recall Information | Centric Compounding Recall |
| Distributed | Direct to consumers, prescribers, & clinics |
| States Affected | Nationwide |
| Number Of Adverse Events | 9 |
| Reported Reactions | Severe headache, nausea, vomiting, fever, chills, chest pain, & malaise |
| Centric Compounding Phone Number | 833-777-6664 |
Tri-Immune Boost & Myer's Cocktail Recalled Glutathione
The Centric Compounding recall matters because it covers Myer’s Cocktail (IV infusion) and Tri-Immune Boost (usually an intramuscular injection). If you received either one, you are inside the recall and may be eligible to file a glutathione injection lawsuit.
Glutathione: Side Effects or Bacterial Endotoxin Reaction
Endotoxin is part of the outer membrane of certain bacteria, and it often survives sterilization. A vial can pass sterility testing while carrying dangerously elevated endotoxin levels. Once injected, it can trigger a catastrophic response from the patient’s immune system within minutes to hours.
32% of patients experienced adverse events from intravenous glutathione.
That figure is legally important because wellness clinics often tell patients with endotoxin exposure that they simply experienced normal side effects.
When compounded injections or IVs have elevated endotoxin levels, patients can suffer significant medical events, including:
Fever, Chills & Uncontrollable Shaking
Sudden fever, chills, and rigor are the most commonly reported reaction, often starting before the infusion is finished.
Shock & Blood Pressure Changes
Endotoxin exposure can cause dangerously low blood pressure changes, and in rare cases, abnormal blood clotting, shock, and death.
Chest Pain & Racing Heart
Tachycardia and chest pain were both reported to the recalling pharmacies and frequently prompted emergency transport.
Severe Headache
A severe headache distinct from an ordinary migraine was reported in connection with all three Texas recalls.
Body Ache & Injection Site Reaction
Diffuse myalgia is common. Pain, swelling, or redness at the injection site points specifically to intramuscular or subcutaneous injection site reactions.
Nausea & Vomiting
Nausea and vomiting often accompany fever and body aches and are easily misdiagnosed as food poisoning or a virus.
Severe Reactions, Shock, & Hospitalization
The CDC confirmed at least three hospitalizations within a month for glutathione-related endotoxin exposure. One patient was admitted to the ICU and treated for shock and abnormal blood clotting, including disseminated intravascular coagulation.
Many patients arrived by ambulance. Emergency room physicians have no way to know endotoxin exposure caused the illness, so the workup chases sepsis-like symptoms of an unknown origin. That gap is why the pharmacy record or infusion receipt matters as much as the medical record.
Adverse Reactions After Intramuscular & Subcutaneous Injections
Patients were injured by glutathione injections, not just IVs. Their adverse events include injection site reactions, pain and swelling, alongside the same responses from immune functions: systemic fever, chills, and body aches. The vial, packaging, and shipping records can all be used as evidence in a glutathione lawsuit.
Lasting Symptoms After an Endotoxin Reaction
Months later, patients report chronic significant medical events, including chronic, severe headaches, photosensitivity, cognitive and processing difficulty, and persistent fatigue. Neurological referral determines whether those symptoms are measurable and likely to continue.
Depending on the severity and permanence, our San Antonio brain injury lawyers who work with neurological experts can accurately calculate long-term damages. The full extent of adverse events from elevated endotoxin levels is still being evaluated.
Who is Eligible to File a Glutathione Injury Lawsuit in Texas
If you or a family member suffered the following adverse events, you may qualify to file a compounded glutathione lawsuit:
- Received IV glutathione, a Myer’s cocktail, a banana bag, or an immune-boost drip in 2026
- Received a glutathione, Tri-Immune Boost, or similar injection
- Received vials shipped to you and injected them yourself
- Got the product at a wellness clinic, med spa, IV bar, mobile service, or workplace visit
- Developed symptoms during or within hours of treatment
- Received emergency room treatment or were hospitalized
- Received a recall notice
- Have chronic symptoms weeks later
- Lost a family member following an infusion or injection
You can still file without the vial or the pharmacy name. We pull the product and recalled lot number from your medical records or the pharmacy’s dispensing records.
How Patients Are Exposed to Bacterial Endotoxins: Clinic & Home-Use
Recalled glutathione reached patients through several channels. The distribution changes who the glutathione lawsuit is filed against.
Glutathione-infused IVs and injections are given at wellness clinics, medspas, IV bars, and by mobile wellness companies that bring the IV drip to the patient. Here, a licensed healthcare provider:
- chose the product name,
- selected the pharmacy,
- screened the patient, and
- monitored the treatment.
Every step is a potential point of negligence, and our San Antonio medication error attorneys examine each.
If recalled glutathione 200 mg/ML, Tri-Immune Boost, or Myer’s Cocktail vials were shipped directly to you, the defendants may include Medisca Inc., the pharmacy, and the healthcare provider who prescribed and arranged the delivery.
A compounded glutathione lawsuit rarely has one defendant, and each link sits under a different body of law. That is why the firm you hire must litigate product liability and medical negligence together, including recall-driven litigation like the Exactech knee recall lawsuits.
Injectable Product/Ingredient Supplier
Medisca, headquartered in New York, supplied the lots at issue. The Food and Drug Administration labels this as “dietary supplement grade.” Glutathione, therefore, isn’t an FDA-approved drug and is not an appropriate ingredient for compounding injectable drugs.
Plaintiffs are suing Medisca Inc. as a “manufacturer” under Texas product liability law, arguing that repackaging, labeling, and distributing dietary supplement-grade material to compounding pharmacies means the company should have known there was a reasonable probability of exactly this problem. The product liability side raises important legal questions that our San Antonio product liability lawyers are prepared to litigate.
Compounding Pharmacy
Pharmacies compounding drugs must use appropriate ingredients for the intended route of each injectable drug. FDA regulations direct these pharmacies to know their suppliers, maintain a lot-specific Certificate of Analysis that includes bacterial endotoxin testing, and build quality into sourcing, stock solution preparation, and final release.
Testing alone isn’t enough. Chapter 797 governs sterile compounding, and three Texas pharmacies have now conducted recalls related to contamination in one lot that was never approved for injection.
The Clinic, Med Spa, or Mobile Service That Administered It
The healthcare provider who injected the patient is often the only party they can name. The provider must weigh the risk of adverse reactions and significant safety concerns of using non-approved injections against the benefits for each patient.
Doctors should never give a glutathione injection if they can’t verify the ingredient grade with the compounding pharmacy. Mobile services carry added exposure because they treat patients with no emergency backup nearby.
We also handle related IV therapy complications, including infiltration claims.
The Prescriber or Platform Behind a Home Delivery
When vials ship directly to the patient, the prescriber who chose the pharmacy has a duty to evaluate the patient’s individual case, disclose that no FDA-approved glutathione product exists, and verify where the pharmacy sourced its ingredient.
They must also notify the patient of a recall. All three pharmacies stated they were contacting patients by telephone, mail, or email, which creates a record of who knew what and when.
Party | Role in the Chain | Which Exposure Pathway | Likely Claim Type | Damage Caps Apply? |
|---|---|---|---|---|
Ingredient supplier | Supplied the recalled lot used to compound the finished product | Both | Product liability | No |
Compounding pharmacy | Compounded the injectable product from that ingredient | Both | Product liability, malpractice, or both | Depends on the individual case |
Clinic, med spa, or mobile service | Selected, prescribed, and administered the product | Clinic only | Malpractice | Yes |
Prescriber or platform | Prescribed and arranged shipment | Home delivery only | Malpractice | Yes |
Product Liability & Medical Malpractice: Why Compounded Glutathione Cases Intersect
Most firms handling these cases know one path or the other. Mass tort pharmaceutical practices will target the supplier, underwork the medical negligence claim, and may miss the Texas malpractice deadlines entirely. A pure malpractice team files against the provider and accepts a recovery limited by Texas’ damage caps.
A compounded glutathione lawsuit requires both investigations running simultaneously.
Texas law recognizes three product defects: manufacturing, design, and marketing or failure to warn. Contamination inside an ingredient lot is a textbook defect, whatever the defense argues about labeling. Product liability claims aren’t subject to the non-economic damage caps that apply to health care cases.
The medical malpractice statute of limitations catches most patients who wait. Plaintiffs must navigate a pre-suit notice and authorization requirement, a 120-day expert report deadline, and a two-year limitations period.
Unless you had vials shipped to you, the medical standard of care a provider owes was likely breached, and you may have a malpractice lawsuit, as well.
You have less time to file. Contact a Texas glutathione lawyer immediately. Call 210-366-4949 to have both tracks evaluated.
Evidence in a Compounded Glutathione Claim
Compounded glutathione cases are won with evidence connecting the vial lot number to a patient on a specific date. The evidence you need depends on how you received the product.
If a clinic or service administered it: invoice or appointment confirmation; consent forms; the medical record and lot documentation; photographs of the vial or packaging; names of others treated at the same session.
If it was delivered to your home: pharmacy invoice and shipping records; the prescription and prescriber name; the box, label, and any remaining vials; the recall notice you received and how it arrived; telehealth intake records.
Either way: EMS run report; emergency room and admission records; labs drawn on presentation; photographs of injection site reactions; text messages or emails with the provider or pharmacy.
Clinics and pharmacies aren’t required to hand records over quickly. Most won’t. Our law firm can compel production. If you’re unsure what the process looks like when a negligent hospital or facility is responsible, we walk you through it.
Compensation For Glutathione Injuries in Texas
Recoverable damages may include:
- Emergency room and ambulance charges
- Hospital admission and intensive care costs
- Specialist and neurology referrals
- Imaging and diagnostic testing
- Future medical expenses
- Lost wages and future earning capacity
- Pain and suffering
- Mental anguish
- Physical impairment
- Loss of consortium
- Funeral and burial expenses in fatal cases
A product with elevated endotoxin levels can cause severe inflammatory reactions, anaphylactic shock, and death. When a patient dies, the family and estate can bring a wrongful death claim and survival action. We represent families pursuing a San Antonio wrongful death claim and patients living with permanent injuries requiring lifetime care.
Over
$0Million
in Verdicts & Settlements Obtained for Our Clients since 2020
Deadlines to File a Glutathione Lawsuit in Texas
The deadline for a compounded glutathione lawsuit depends on the type of case:
Claim Type | Defendant | Deadline |
|---|---|---|
Product liability | Ingredient supplier, compounding pharmacy | 2 years from injury |
Health care liability claim | Clinic, prescriber, pharmacy if characterized as a provider | 2 years (Expert report due within 120 days of answer) |
Wrongful death | Any responsible party | 2 years from date of death |
Survival action | Any responsible party | 2 years |
Any responsible party | Tolled, with different rules under Chapter 74 | |
Statute of repose | Manufacturing defendant | 15 years from date of sale (Not a concern in a 2026 exposure) |
Legal Process For Glutathione Cases
- Free consultation to discuss your case with a Texas Glutathione lawyer
- Identification of the compounding source through clinic, pharmacy, or shipping records
- Medical record collection and expert review
- Notice and claim filing
- Negotiation and trial if the defense will not offer a fair settlement
Why Hire an Elite, Board-Certified Texas Glutathione Lawsuit Attorney From Janicek Law
This litigation punishes firms that only know one area of law. Beth Janicek’s board certification in personal injury trial law reflects a standard a small fraction of Texas attorneys meet.
For over 30 years, our firm has recovered more than $85 million for injured clients, handling both catastrophic product cases and complex medical negligence claims. We take these cases on contingency, so there is no fee unless we recover. Read what clients say about working with our team.
Filing Glutathione IV & Injection Lawsuits Across Texas
All three recalling pharmacies are Texas pharmacies, and the outbreak was first identified by the Texas Department of State Health Services, so Texas is central to the litigation no matter where patients live. The CDC has confirmed cases in Texas, Washington, Florida, and New York, and the Optimal Balance Pharmacy product alone reached 14 states.
Wellness and IV clinics cluster in Stone Oak, Alamo Heights, the Medical Center district, Downtown, and the Northwest Side. Mobile services operate across all of San Antonio and Bexar County.
Centric Compounding and Optimal Balance Pharmacy are both Houston pharmacies, so claims are filed in Harris County district court. The Texas Medical Center corridor carries one of the densest concentrations of wellness and infusion providers in the state. If you were injured by glutathione from Centric Compounding or Optimal Balance Pharmacy in Houston, our attorneys are ready to help.
Victory Medical Center Pharmacy is an Austin pharmacy, so claims against it sit in the Travis County district courts. If you were shipped vials or treated with product from Victory Medical Center Pharmacy in Austin and suffered an adverse event, contact a glutathione attorney for a free consultation.
Patients Across The Country
Patients in Washington, Florida, and New York should know that the defendants are Texas-based. Contact our law firm to see how we can help! Call 210-366-4949.
Not seeing your city? We may still take the case. Contact us or call 210-366-4949.
Compounded Glutathione Lawsuit FAQ
I got a glutathione injection, not an IV. Do I still have a case?
Yes, you may still have a case if you got an injection. The CDC confirmed patients were affected by contaminated glutathione both intravenously and through injection. A glutathione injection lawsuit follows the same process as an IV claim.
The vials were shipped to my house, and I injected glutathione myself. Who do I sue?
If the vials were shipped and you administered glutathione injectable drugs yourself, you can potentially sue the ingredient supplier, the compounding pharmacy, and whoever prescribed the product and arranged the shipment. No clinic is required for a claim, and self-administration does not make the contamination your fault.
Can I file a glutathione lawsuit if I don't know which pharmacy made it?
Yes, you can file a glutathione lawsuit if you don’t know which pharmacy compounded it. Medical records, pharmacy receipts or invoices, and shipping records identify the compounder and the lot number. Obtaining those records is part of the case workup, not something you need before you call.
What if my lot number is not on a recall list?
If the lot number isn’t on the glutathione recall list, you may still have a claim. Only certain lots have been identified and the investigation is ongoing. You can report the reaction to FDA’s MedWatch program. If you have any questions about your lot number, an attorney from our firm can help you get answers,
What if I signed a waiver at the clinic?
If you signed at a clinic, this doesn’t necessarily stop you from filing a claim. Consent forms don’t wave claims against ingredient suppliers or pharmacies. Their effect on the administering provider depends on the specific terms and how that provider handled their duty when sourcing lots of compounded glutathione and using glutathione injectable drugs that weren’t approved for injecting.
Do I have a case if I was treated and released the same day?
Yes, you may potentially have a case if you were released the same day. Severity affects your claims’s value, not whether you qualify to file a glutathione lawsuit. Some injured patients what were immediatey released experience chronic symptoms that persist for months. Endotoxin reactions are sometimes misdiagnosed as a panic attack or a viral illness.
What does it cost to hire a lawyer for glutathione injuries?
If doesn’t cost you anything to hire a lawyer for glutathione injuries. Our firm offers free consultations; you don’t pay unless we recover compensation for you.
Call 210-366-4949.
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