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[Recalled] Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation an

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

ProductNylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurolo
Brand / manufacturerRiverpoint Medical, LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2761-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date05 August 2016

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.

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 Riverpoint Medical, LLC

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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