- Recalling firm
- Medical Action Industries, Inc. 306
- Reason for recall
- Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
- Affected products (lot / model / serial)
- REF/UDI-DI/Lot(Expiration Date): 59553/10809160010518/330274(9/1/2026), 331036(11/1/2026), 332995(11/1/2026), 333957(11/1/2026), 338894(11/1/2026); 83945B/10809160444269/330827(10/10/2026), 330907(10/10/2026), 333956(11/1/2026), 350340(11/1/2026), 351266(11/30/2026), 373674(5/31/2027)
- Units affected
- 3,606
- Distribution pattern
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- 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-3107-2026
- Recall initiated
- July 23, 2026
- FDA classification date
- September 9, 2026
- FDA report date
- September 16, 2026
- FDA event ID
- 99613
- Last updated on HTM Vibe
- September 23, 2026