Glutathione Injection

  • Potential elevated endotoxin levels
  • Company: Greenwich Rx
  • Drugs
  • FDA
  • October 1, 2026

Product details

  • Glutathione Injection

Company announcement

Greenwich Rx is voluntarily recalling specific lots of its compounded glutathione due to potential elevated endotoxin levels.

The product was distributed to patients nationwide between June 26, 2026, and September 21, 2026.

Two patients have reported receiving emergency department care following intravenous administration of a glutathione product not formulated for IV use.

Risk:

There is reasonable probability that injectable products with elevated endotoxin levels could cause significant medical events including fevers, hypotension, inflammatory reactions, anaphylactic shock and death. To date, Greenwich Rx has received two reports involving patients who received emergency department care following intravenous (IV) administration of a glutathione product that was not formulated for IV use.

Impacted states: Nationwide

Products:

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

- Glutathione Injection

Contact

For more information, call (866) 552-4916 or email GreenwichRx7542@sedgwick.com.

View the original FDA notice

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