Official recall notice

FDA DrugClass IINotable

FDA Recall: PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured

Recall date
2026-08-26
Category
Drug
FDA class
Class II

Why it was recalled

Hazard

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

Product description

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

Affected products

Lot: P400157, Exp 08/31/2026; Lot PA00047A, Exp 09/30/2027

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