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FDA
Food and Drug Administration · Recall Z-2922-2026 · Jun 24, 2026

Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX

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 II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX

Affected identifiers

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

Model S8698GX UDI-DI 20612479214716 Lot D5M3438FYUPC 20612479214716

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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.