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FDAFebruary 3, 2022drug

Morphine Sulfate PF 25 mg/25mL (1 mg/mL) in NaCl, 25 mL in 30 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0105-04.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A

What to do

FDA enforcement status: Terminated

Brands named

staq pharmastaq

UPCs

73177010504

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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