[Recalled] Olympus DISPOSABLE GRASPING FORCEPS, FG-51D — Forceps do not comply with Olympus standards for the amount of force required t… | FDA 2022-03-31

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Olympus Corporation of the Americas

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• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. — Class II
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. — Class II
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190 — Class I
• Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.