Argon Medical recalls Arterial Line Kit 20ga x 6 (REF 400115A) due to potential sterility issues. Affected units have specific lot numbers expiring July 2027. Consumers should contact the company for details.
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Argon Medical is recalling Arterial Line Kits with 20-gauge catheters that may not meet sterility standards. This could lead to infections if used improperly. The recall affects specific lot numbers sold between 2023 and 2027.
The kits contain Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules that were not properly tested for sterility. If these ampules are contaminated, they could cause infections when used in medical procedures.
Healthcare professionals using the Arterial Line Kit 20ga x 6 with lot numbers ending in 20886333212884 to 20886333212885 or 20886333212880. Patients receiving these kits during medical procedures are at risk of infection.
Check the box label for the reference number 400115A and lot numbers ending in 20886333212884, 20886333212885, or 20886333212880. The kits expire by July 19, 2027.
Look for the reference number 400115A and lot numbers ending in 20886333212884, 20886333212885, or 20886333212880 on the box.
Reach out to Argon Medical Devices, Inc for further instructions on handling the recalled product.
The kits contain Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules that did not meet sterility release criteria.
Check the product label for the reference number 400115A and lot numbers ending in 20886333212884, 20886333212885, or 20886333212880. Contact Argon Medical Devices, Inc for further instructions.
Yes, if the ampules are contaminated, they could cause infections during medical procedures.
We’ve drafted a message you can send Argon Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2708-2026 — Argon Medical Argon Medical Hello, I own a Argon Medical that is covered by recall Z-2708-2026 from Argon Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
