FDA Drug Recalls

Recalls / Class II

Class IID-1113-2023

Product

rocuronium 50 mg/5 mL (10 mg/mL), 5 mL Syringes, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue, Pheonix, AZ, NDC 72196-6010-1.

Affected lot / code info
Lot# 36-262729, 36-262982, 36-262981, 36-262732, 36-262731, 36-262730, Exp 10/11/2023 ;

Why it was recalled

Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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
3519 Syringes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2023-08-17
FDA classified
2023-08-28
Posted by FDA
2023-09-06
Terminated
2025-03-27
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1113-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.