SeriousFDAOngoing
Can cause serious harm or death.
Arterial Line Kit 20ga x 6, REF: 400115A
Check the device or its packaging for
REF/UDI-DI Box:Unit/Lot(Expiration): 400115A/20886333212884:00886333212880/11655174(7/19/2027), 11655183(7/19/2027), 11655185(7/19/2027), 11659131(7/19/2027);
- Why
- Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- Distributed
- Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.
- Company
- Argon Medical Devices, Inc
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2708-2026 · retrieved 10 July 2026
Read the official notice