- Recalling firm
- Medical Action Industries, Inc. 306
- Reason for recall
- Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
- Affected products (lot / model / serial)
- UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
- Units affected
- 2030 kits
- Distribution pattern
- US distribution to state of: AZ OUS: None
- Firm location
- Arden, NC, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2007-2026
- Recall initiated
- March 17, 2026
- FDA classification date
- May 6, 2026
- FDA report date
- May 13, 2026
- FDA event ID
- 98698
- Last updated on HTM Vibe
- July 24, 2026