FDA
Food and Drug Administration · Recall Z-2708-2026 · Jun 1, 2026Arterial Line Kit 20ga x 6, REF: 400115A
Argon Medical Devices, Inc
The 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. FDA Class I recall.
The remedy
Follow FDA guidance
About this recall
Arterial Line Kit 20ga x 6, REF: 400115A
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model 11655183(7/19/2027)Model 11655185(7/19/2027)Model 11659131(7/19/2027)UPC 20886333212884UPC 00886333212880Would you have heard about this one?
RapidRecall watches everything you own against every new federal recall and emails you the moment something you bought turns up. Free for your most important items.
Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.