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Verified · FDAClass II — Possible RiskMedications

Greenwich Rx Issues Voluntary Nationwide Compounded Glutathione Recall 2026

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

Greenwich Greenwich Rx Issues Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels — recalled per FDA on 10/1/2026. Reason: Potential elevated endotoxin levels.

Agency
FDA
Issued
Oct 1, 2026
Brand
Greenwich
States affected
1
What to do right now

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.

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Verified summary of the official U.S. Food and Drug Administration notice · Issued October 1, 2026 · Last synced Oct 22, 2026

What's recalled

Company: Greenwich Rx Brand(s): Greenwich Glutathione Injection

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Why it was recalled

Potential elevated endotoxin levels

Where was it sold
1 state
nationwide
Official noticefda.gov
More recalls like this
4 related — by brand, contaminant, and category

Frequently asked questions

Is the Greenwich recall still active?

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

How do I know if my Greenwich is affected?

All units of Greenwich matching the description above are affected.

What should I do if I have the recalled Greenwich?

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