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FDA (Device enforcement)Recalled 2026-06-01class i

Argon Medical Devices, Inc: Arterial Line Kit 20ga x 6, REF: 400115A

Hazard

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Details from the source

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. Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. Quantity: 440 Lot/code info: 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);

UPC codes

20886333212884, 00886333212880

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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