FDAHealthJune 1, 2026

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

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

Is this relevant to me?

Geography: Nationwide
Source agency: FDA
Category: Health
Published: June 1, 2026

Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.

What's affected?

Product: Arterial Line Kit 20ga x 6, REF: 400115A
Brand: Argon Medical Devices, Inc
Lot code: (Expiration):

Additional details

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);

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 440.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.