- Recalling firm
- Argon Medical Devices, Inc
- Reason for recall
- Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- Affected products (lot / model / serial)
- REF/UDI-DI Box:Unit/Lot(Expiration): 008416A/20886333217636:00886333217632/11656898(7/19/2027); 008566A/20886333217643:00886333217649/11654475(12/31/2026), 11654478(7/19/2027)
- Units affected
- 950
- Distribution pattern
- Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.
- Firm location
- Athens, TX, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2704-2026
- Recall initiated
- June 1, 2026
- FDA classification date
- July 10, 2026
- FDA report date
- July 22, 2026
- FDA event ID
- 99069
- Last updated on HTM Vibe
- July 28, 2026