[Recalled] DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony gr
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft |
|---|---|
| Brand / manufacturer | DePuy Mitek, Inc., a Johnson & Johnson Co. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2619-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 12 May 2017 |
| EAN / barcode | 10886705026944 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
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.