medical MODERATE Updated 2026-08-19

Covidien, LP recalls Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623

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Recalled Product

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

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: SP-623 UDI-DI 20884521037073 Lot D6A2963Y

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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View official government recall

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