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[Recalled] PIPELINE LS ACCESS SYSTEM, 3rd Dilator, 14 mm Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor. — Dilators and H

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductPIPELINE LS ACCESS SYSTEM, 3rd Dilator, 14 mm Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
Brand / manufacturerDePuy Spine, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0095-2014
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date31 July 2013
EAN / barcode287105014

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

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 DePuy Spine, 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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