FDA Recalls, Market Withdrawals & Safety AlertsOther

Glutathione Injection

Recall fda-alert:2026-10-01:Greewich:Glutathione InjectionPublished 2026-10-01Company Greenwich Rx
ReasonPotential elevated endotoxin levels
DistributionThis field was not provided in the official notice. Please confirm in the original notice.
Code informationThis field was not provided in the official notice. Please confirm in the original notice.
i

Official-information notice
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

Review the fields published in the original agency record.

Recall number

fda-alert:2026-10-01:Greewich:Glutathione Injection

Classification

Other

Published

2026-10-01

Recalling firm

Greenwich Rx

Product description

Glutathione Injection

Product code

This field was not provided in the official notice. Please confirm in the original notice.

Code information

This field was not provided in the official notice. Please confirm in the original notice.

Product quantity

This field was not provided in the official notice. Please confirm in the original notice.

Distribution

This field was not provided in the official notice. Please confirm in the original notice.

Reason for recall

Potential elevated endotoxin levels

Need the original notice?
Open the agency source for the complete official notice and any disposal, return, or contact instructions.

Open official source ↗

← Return to Foods Recall search

Editorial review: Foods Recall Editorial Team
Last synchronized: 2026-10-01. Foods Recall does not replace agency guidance.