- 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)
- UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)
- Units affected
- 1,960
- 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-3106-2026
- 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