FDA Drug Recalls

Recalls / Class II

Class IID-0065-2024

Product

Foscarnet Sodium 2.4mg/0.1 mL solution for injection, 0.2 mL single-dose Staclear Luer Slip Syringe, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

Affected lot / code info
Lot #: 68680, Exp. Date 12/4/2023

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
136 syringes
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-0065-2024. 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