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Verified · FDAClass I — Health RiskMedications

Glutathione Injection , 200 mg/mL, 10 mL multi-dose vial, Rx only Recall 2026

Greenwich RxIssued October 1, 2026Updated Reviewed by the Recall Watch editorial team

Greenwich Rx Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx. — recalled per FDA on 10/1/2026. Reason: Microbial Contamination of Sterile Products.

Agency
FDA
Issued
Oct 1, 2026
Brand
Greenwich Rx
Distribution
1 states
Lots affected
20
What to do right nowHigh risk

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

Verified summary of the official U.S. Food and Drug Administration notice · Issued October 1, 2026 · Last synced Nov 2, 2026

What's recalled

Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx.

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Why it was recalled

Microbial Contamination of Sterile Products

Affected products & lot numbers
20 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot # 0060-062426-1
BUD: 10/02/2026
Lot # 0060-062726-1
BUD: 10/05/2026
Lot # 0060-070926-1
BUD: 10/17/2026
Lot # 0060-071426-1
BUD: 10/22/2026
Lot #0060-071426-2
BUD: 10/22/2026
Lot # 0060-072026-1
BUD: 10/28/2026
Lot # 0060-072726-1
BUD: 11/04/2026
Lot #0060-072926-1
BUD: 11/06/2026
Lot # 0060-073126-1
BUD: 11/08/2026
Lot # 0060-080426-1
BUD: 11/12/2026
Where was it sold
1 state

US Nationwide in th USA

nationwide
Official noticefda.gov
More recalls like this
4 related — by brand, contaminant, and category

Frequently asked questions

Is the Greenwich Rx recall still active?

Yes, this recall is currently active as of October 1, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot # 0060-062426-1, BUD: 10/02/2026, Lot # 0060-062726-1, BUD: 10/05/2026, Lot # 0060-070926-1, BUD: 10/17/2026, Lot # 0060-071426-1, BUD: 10/22/2026, Lot #0060-071426-2, BUD: 10/22/2026, Lot # 0060-072026-1, BUD: 10/28/2026, Lot # 0060-072726-1, BUD: 11/04/2026, Lot #0060-072926-1, BUD: 11/06/2026, Lot # 0060-073126-1, BUD: 11/08/2026, Lot # 0060-080426-1, BUD: 11/12/2026. Check the label on your product.

What should I do if I have the recalled Greenwich Rx?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.