FDA Drug Recalls

Recalls / Class II

Class IID-0411-2024

Product

labetalol HCl 20 mg/4mL Injection, (Concentration=5 mg/mL), 4 mL fill Syringe, Rx Only, SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0700-28, Bar Code 70004070028

Affected lot / code info
Lot #: 1223047334 Exp 12/23/23; 1223048170 Exp 02/01/24

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
SCA Pharmaceuticals, LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
755 Rainbow Rd Ste B, N/A, Windsor, Connecticut 06095-1024

Distribution

Quantity
2,458, syringes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2023-11-09
FDA classified
2024-03-22
Posted by FDA
2024-04-03
Terminated
2024-08-27
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0411-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls