CLASS II ONGOING Drug recall · Reported 5 Mar 2025 · FDA Enforcement Report
ViaMed Alcohol Prep Pads, For External Use Only recalled
Wuxi Medical lnstrument Factory is recalling ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile per, 100, distributed in Florida. The recall was initiated on 12 Feb 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0247-2025
- FDA event ID
- 96210
- Recalling firm
- Wuxi Medical lnstrument Factory, Wuxi, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 12 Feb 2025
- FDA classified
- 21 Feb 2025
- Reported
- 5 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
Timeline
| 12 Feb 2025 | Recall initiated by company | |
| 21 Feb 2025 | Classified by FDA | +9 days |
| 5 Mar 2025 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
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.
Where it was distributed
FL
Questions about this recall
Why was it recalled?
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Which lots are affected?
Lot #s: 200830, Exp 08/29/2025; 210925, Exp 09/24/2026; 221225, Exp 12/24/2027.
Where was it sold?
FL
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.