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FDA
Food and Drug Administration · Recall Z-2921-2026 · Jun 24, 2026

Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623

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

Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623

Affected identifiers

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

Model SP-623 UDI-DI 20884521037073 Lot D6A2963YUPC 20884521037073

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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.