FDA Drug Recalls

Recalls / Class II

Class IID-0397-2022

Product

Ceftazidime, Sterile Ophthalmic Solution for Injection, Preservative Free (11.25 mg/0.5 mL (22.5 mg/mL), 0.5mL single use syringe for Intraocular Injection, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-0733-01

Affected lot / code info
09-2021-01@6 12/14/2021 & 10-2021-27@4 01/01/2022

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Edge Pharma, LLC
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
856 Hercules Dr, Colchester, Vermont 05446-8014

Distribution

Quantity
168 syringes
Distribution pattern
nationwide

Timeline

Recall initiated
2021-12-06
FDA classified
2022-01-24
Posted by FDA
2022-02-02
Terminated
2023-06-07
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0397-2022. 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