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PEMRYDI RTU(pemetrexed injection) recall

Shilpa Medicare Limited recalled PEMRYDI RTU(pemetrexed injection) on August 26, 2026 because of discolored solution. It was sold nationwide.

Why it was recalled

Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials

What's recalled

PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2461-1

Quantity: 9,489 50mL vials

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Shilpa Medicare Limited, Jadcherla, Mahabubnagar District
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Nationwide in the USA.
Status
Ongoing
Recall number
D-0765-2026
Source
U.S. Food and Drug Administration

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