FDA Drug Recalls

Recalls / Class II

Class IID-0431-2022

Product

CSF Otic Insufflation Capsule, Sulfacetamide Sodium/ Ciprofloxacin/ Amphotericin B Otic Powder, 50mg / 30mg / 5mg, 5 count bottle, For Otic Use with Insufflator, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1633-05

Affected lot / code info
10-2021-27@8 01-25-2022

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
1055 bottles
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-0431-2022. 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