FDA Drug Recalls

Recalls / Class II

Class IID-0242-2023

Product

VITAMIN D3-AQUEOUS- 10,000IU/ML (1ML VIAL) INJECTABLE; VITAMIN D3-PF-ETHYL OLEATE- 50,000IU/ML (1ML VIAL) INJECTABLE, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.

Affected lot / code info
t20221017@25 t20221013@15

Why it was recalled

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Recalling firm

Firm
Pharmacy Innovations
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
2936 W 17th St, N/A, Erie, Pennsylvania 16505-3929

Distribution

Quantity
N/A
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2022-12-22
FDA classified
2023-01-26
Posted by FDA
2023-02-01
Terminated
2024-07-31
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0242-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.