STAQ Pharma, Inc. recalls 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., Den

Recalled February 23, 2022 · FDA recall D-0633-2022 · STAQ Pharma

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 · FDA Class I

Units

905 Syringes

Sold at

CO, OH, and TX.

Description

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

Product

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.

Manufacturer(s)

STAQ Pharma, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →