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Medical Device

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

Recall date: 2026-08-19 · Source: FDA_DEVICE
Brand / Firm
Covidien, LP
Product
Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
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 SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
View official recall notice →