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FDA
Food and Drug Administration · Recall Z-2706-2026 · Jun 1, 2026

General Biospy Tray, REF: GUTS1000

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

General Biospy Tray, REF: GUTS1000

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

UPC 20886333001594UPC 00886333001590

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.