medical MODERATE Updated 2026-09-02

Olympus Corporation of the Americas recalls POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer

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Recalled Product

POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories

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Hazard / Issue

Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902.

✅ 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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