FDA
Food and Drug Administration · Recall Z-3035-2026 · Aug 18, 2026POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Olympus Corporation of the Americas
The hazard
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
UPC 00821925044531Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.