- Recalling firm
- Medical Action Industries, Inc. 306
- Reason for recall
- Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.
- Affected products (lot / model / serial)
- UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)
- Units affected
- 657
- Distribution pattern
- US: AZ, CO
- Firm location
- Arden, NC, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2792-2026
- Recall initiated
- May 13, 2026
- FDA classification date
- July 30, 2026
- FDA report date
- August 5, 2026
- FDA event ID
- 99337
- Last updated on HTM Vibe
- August 11, 2026