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Medical Device

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

Recall date: 2026-08-19 · Source: FDA_DEVICE
Brand / Firm
Covidien, LP
Product
Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX
Reason for recall
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.
Units affected
135,875 total
Description
Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX
View official recall notice →