FDARecall 99530Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.
Is it yours? Products and codes
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
- Lot or code
- Lot: P400172; Lot PA00050A, Exp 09/30/2027
- FDA recall number
- D-0764-2026
- Quantity
- 18,434 10mL vials
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
- Lot or code
- Lot: P400157, Exp 08/31/2026; Lot PA00047A, Exp 09/30/2027
- FDA recall number
- D-0765-2026
- Quantity
- 9,489 50mL vials
Distribution (FDA): Nationwide in the USA.
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Shilpa Medicare Limited
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.