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Health & beauty United States Recall (ongoing)

Olympus Corporation of the Americas recalls POWERSEAL 5 MM

The POWERSEAL 5 mm (diameter), 23 cm long Curved Jaw Sealer & Divider, Double Action (Model PS-0523CJDA, UDI-DI 00821925044531, Lot FR490902) is being recalled. The recall is due to a potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.

What's being recalled

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

Recalling firm: Olympus Corporation of the Americas, Center Valley, PA, United States.

How to identify it

Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902.

The hazard

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

What to do

Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.

The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.

Where it was sold

Worldwide - US Nationwide distribution in the states of Kansas and Florida. The countries of Australia, European Union, Japan.

The official notice

This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.

Read the official notice (opens in a new tab)

A little guidance

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