FDAFDA · Food and drugs·Recall number D-0765-2026
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
Published August 26, 2026 · Recall initiated: July 29, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PEMRYDI RTU
- Manufacturer
- Shilpa Medicare Limited
- Distributor
- Nationwide in the USA.
- UPC
- 0370121246213
- Lot
- Lot: P400157, Exp 08/31/2026; Lot PA00047A, Exp 09/30/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- India
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