- Recalling firm
- Windstone Medical Packaging, Inc.
- Reason for recall
- Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
- Affected products (lot / model / serial)
- UDI/DI none, Lot Codes: 237663, 237901, 237957, 238041, 238084, 238085, 238146, 238197, 238589, 239157, 239216, 239286, 239337, 239386, 239943, 240269, 240633, 240705, 240903, 240904, 241034, 241223, 241224, 241313.
- Units affected
- 45 units
- Distribution pattern
- US Nationwide distribution in the states of PA, GA, CA, WA.
- Firm location
- Billings, MT, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2622-2026
- Recall initiated
- May 21, 2026
- FDA classification date
- July 1, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 99189
- Last updated on HTM Vibe
- July 23, 2026