FDA Drug Recalls

Recalls / Class II

Class IID-0435-2022

Product

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

Affected lot / code info
08-2021-03@8 12-31-2021 & 09-2021-07@10 02-04-2022

Why it was recalled

CGMP Deviations

Recalling firm

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

Distribution

Quantity
20 vials
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-0435-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.