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Olympus Corporation of the Americas recalls POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting
Recalled September 2, 2026 · FDA recall Z-3035-2026 · Olympus Corporation of the Americas
Hazard
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. · FDA Class II
Units
335 units
Sold at
Worldwide - US Nationwide distribution in the states of Kansas and Florida. The countries of Australia, European Union, Japan.
Description
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
Product
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →