D-0435-2022 Class II Terminated
FDA drug recall D-0435-2022 was initiated by Edge Pharma, LLC on December 6, 2021 and is designated Class II. Reason for recall: CGMP Deviations The recall status is terminated (terminated June 7, 2023). Affected quantity: 20 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
- 20 vials
Product Description
Dibutyl Squaric Acid, Topical Solution (PF) Multiple Dose Vial, 1%, 10 mL per vial, Edge Parma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1156-03
Reason for Recall
CGMP Deviations
Distribution Pattern
nationwide
Code Information
08-2021-03@8 12-31-2021 & 09-2021-07@10 02-04-2022