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[Recalled] PDS Plus Antibacterial Suture-PDS PLUS Undyed Suture 45cm (18") 5-0 Single Armed P-3 Prime Needle Product Code: PDP493G (GTIN 10705031203945) — Products do not meet a tensile strength specification | FDA 2018-06-08

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

ProductPDS Plus Antibacterial Suture-PDS PLUS Undyed Suture 45cm (18") 5-0 Single Armed P-3 Prime Needle Product Code: PDP493G (GTIN 10705031203945)
Brand / manufacturerEthicon, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2533-2018
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date08 June 2018
EAN / barcode10705031203945

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Products do not meet a tensile strength specification

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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