- Recalling firm
- Medical Action Industries, Inc. 306
- Reason for recall
- Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
- Affected products (lot / model / serial)
- Lot Code: Lot No.: 327075 328690 319980 320965 318461 322375 325653 330775 331356 336680 UDI: 20809160242558
- Units affected
- 3740 kits (180 cases)
- Distribution pattern
- US Nationwide distribution in the state of CA.
- Firm location
- Arden, NC, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2858-2026
- Recall initiated
- May 21, 2026
- FDA classification date
- August 3, 2026
- FDA report date
- August 12, 2026
- FDA event ID
- 99338
- Last updated on HTM Vibe
- August 18, 2026