FDA Drug Recalls

Recalls / Class II

Class IID-0051-2024

Product

Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection, 0.8 ML Single Dose Vial, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

Affected lot / code info
Lot #: 69985, exp. date 11/15/2023

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Pine Pharmaceuticals, LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
355 Riverwalk Pkwy, N/A, Tonawanda, New York 14150-5837

Distribution

Quantity
26 vials
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2023-10-02
FDA classified
2023-10-19
Posted by FDA
2023-10-25
Terminated
2024-05-15
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0051-2024. 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