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[Recalled] Coated VICRYL RAPIDETM (Polyglactin 910) Suture — On August 17, 2017, Ethicon had decided to initiate a medical device recall (re… | FDA 2017-08-17

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

ProductCoated VICRYL RAPIDETM (Polyglactin 910) Suture
Brand / manufacturerEthicon, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0693-2018
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date17 August 2017
EAN / barcode10705031149168

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: On August 17, 2017, Ethicon had decided to initiate a medical device recall (removal) of the twenty-five (25) lots of VICRYL RAPIDETM (Polyglactin 910) Suture that were distributed to the field. During finished goods testing, a suture damage was identified on a lot of VICRYL RAPIDETM Suture. During the course of the subsequent investigation, the suture also failed knot tensile strength testing.

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 Ethicon, 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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