- 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): BMT1104STL/20886333007862:00886333007868/11650679(11/30/2026); BMET1104TL/20886333007602:00886333007608/11654764(3/31/2028); BMT1104CATL/20886333007763:00886333007769/11650887(11/30/2026)
- Units affected
- 850
- 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-2707-2026
- 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