Where's it on?
FDA · Drugs ·

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), 100 mg/10 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: 70121-2453-1

Quantity: 18,434 10mL 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