D-0414-2022 Class II Terminated
FDA drug recall D-0414-2022 was initiated by Edge Pharma, LLC on December 6, 2021 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated June 7, 2023). Affected quantity: 2463 vials.
Recall Details
- Product Type
- Drugs
- Report Date
- February 2, 2022
- Initiation Date
- December 6, 2021
- Termination Date
- June 7, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2463 vials
Product Description
Phenylephrine HCl / Tropicamide / Ciprofloxcin / Ketorolac Sterile Ophthalmic Solution, 10%/1%/0.3%/0.125%, 0.8 mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1270-01
Reason for Recall
Lack of Assurance of Sterility
Distribution Pattern
nationwide
Code Information
08-2021-31@8 12/21/2021 & 10-2021-13@1 01/19/2022