ViaMed Alcohol Prep Pads — Class II drug recall D-0247-2025
Ongoing recall by Wuxi Medical lnstrument Factory Co., Ltd., reported 2025-03-05, distributed in FL. Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
| Recall number | D-0247-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wuxi Medical lnstrument Factory Co., Ltd., Wuxi, N/A, China |
| Recall initiated | 2025-02-12 |
| Classified | 2025-02-21 |
| Reported by FDA | 2025-03-05 |
| Distributed | FL |
| Quantity | 37,500 boxes |
| Reason classes | sterility, cgmp |
| NDC | 70006-0500-01 |
| Lot numbers | 200830, 210925, 221225 |
| Expiration dates | 2025-08-29, 2026-09-24, 2027-12-24 |
Product
ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in China, Manufactured for: Rece International Corp., Miami Lakes, FL, 33014, USA, NDC: 70006-500-01.
Reason for recall
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0247-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.