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FDA
Food and Drug Administration · Recall Z-2709-2026 · Jun 1, 2026

Bone Marrow Tray, REF: CB0033TL; CB0355TLA

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

Bone Marrow Tray, REF: CB0033TL; CB0355TLA

Affected identifiers

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

Model 11652276(3/31/2028)Model CB0355TLA/20886333217698:00886333217694/11651977(3/31/2028)UPC 20886333217308UPC 00886333217304UPC 20886333217698UPC 00886333217694

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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.