D-0435-2022 Class II Terminated

Recalled by Edge Pharma, LLC — Colchester, VT

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