- Recalling firm
- AVID Medical, Inc.
- Reason for recall
- Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.
- Affected products (lot / model / serial)
- Lot Number:1658438 7/31/2026 UDI: 10809160460481
- Units affected
- 98 Kits
- Distribution pattern
- US Nationwide distribution in the state of NE.
- Firm location
- Toano, VA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3109-2026
- Recall initiated
- July 14, 2026
- FDA classification date
- September 4, 2026
- FDA report date
- September 16, 2026
- FDA event ID
- 99525
- Last updated on HTM Vibe
- September 23, 2026