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FDAFDA · Food and drugs·Recall number D-0633-2022

HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.

Published February 23, 2022 · Recall initiated: February 3, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's 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

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
STAQ Pharma, Inc.
Distributor
CO, OH, and TX.
Lot
Lot Number: 21104221A, Expiration date: 05-22-2022
Risk classification
Class I
Area (FDA)
drug
Country
United States

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