FDA Drug Recalls

Recalls / Class II

Class IID-0952-2023

Product

glycopyrrolate 1 mg/5 mL (0.2 mg/mL), For Anesthesia Use, Syringe, RX ONLY, CAPS, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6084-1

Affected lot / code info
Lot: 36-247022, Exp 08/07/2023; 36-239877, Exp 07/13/2023; 36-241448, Exp 07/20/2023; 36-251782, Exp 08/29/2023

Why it was recalled

Lack of assurance of sterility. Validation data for decontamination cycles is lacking.

Recalling firm

Firm
Central Admixture Pharmacy Services, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2200 S 43rd Ave, N/A, Phoenix, Arizona 85043-3909

Distribution

Quantity
770 Syringes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2023-07-14
FDA classified
2023-08-01
Posted by FDA
2023-08-09
Terminated
2025-03-28
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0952-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.