US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 6, 2023 (3 years ago)

GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Label Mix-up

What was recalled

GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3

Recalling firm
HF Acquisition Co LLC
NDC code
51662-1487-3
Origin
WA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0870-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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