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FDA
Food and Drug Administration · Recall Z-2920-2026 · Jun 24, 2026

Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31

Covidien, LP

The hazard

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31

Affected identifiers

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

UPC 10884521070912UPC 20884521070919UPC 20884521071060

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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.