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[Recalled] 8MM RESANO FORCEPS,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments. — Deviations in reprocessing steps from those stated in the reprocessing instruct… | FDA 2014-11-03

recall fda device united-states

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

Product8MM RESANO FORCEPS,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
Brand / manufacturerIntuitive Surgical, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0435-2015
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date03 November 2014

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Deviations in reprocessing steps from those stated in the reprocessing instructions can cause surface degradation of the housing and/or accelerate mechanical wear of the instrument.

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 Intuitive Surgical, Inc.

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.

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