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[Recalled] SpiraLok 6.5mm with Ethibond and needles Product Number: 222962 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and e

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductSpiraLok 6.5mm with Ethibond and needles Product Number: 222962 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
Brand / manufacturerDePuy Mitek, Inc., a Johnson & Johnson Co.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0142-2013
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date06 September 2012

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Fracture of SPIRALOK Anchors post op, requiring patient revision

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 Mitek, Inc., a Johnson & Johnson Co.

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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