D-0429-2025 Class II Terminated
FDA drug recall D-0429-2025 was initiated by KENIL HEALTHCARE PRIVATE LIMITED on April 24, 2025 and is designated Class II. Reason for recall: CGMP Deviations The recall status is terminated (terminated February 19, 2026). Affected quantity: 9,336 Tubes.
Recall Details
- Product Type
- Drugs
- Report Date
- May 28, 2025
- Initiation Date
- April 24, 2025
- Termination Date
- February 19, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9,336 Tubes
Product Description
Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc/ Neomycin Sulfate/ Polymyxin B Sulfate, Net Wt 2 oz (56g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, Made in India, NDC 55758-440-02, UPC 8 10096 77162 9.
Reason for Recall
CGMP Deviations
Distribution Pattern
DE and NC
Code Information
Lot SP27A, Exp: 09/30/2026