FDA Device recall Z-2616-2017
DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat rec…
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat rec… by Depuy Mitek A Johnson And Johnson, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2616-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-12 |
| Published | 2017-06-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Depuy Mitek A Johnson And Johnson |
| Distribution | AZ, CA, CO, GA, MA, MI, OH, WA |
Product
DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
Reason
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
Identifiers
| code_info | GTN: 01)10886705026791 Lot Codes: 16C01, 16E01, 16E02, 16E03, 17B01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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FDA Device · Class II · 2023-06-14 · Depuy Mitek A Johnson And Johnson - DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobiliza…
FDA Device · Class II · 2023-06-14 · Depuy Mitek A Johnson And Johnson - DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilizat…
FDA Device · Class II · 2023-06-14 · Depuy Mitek A Johnson And Johnson
All Depuy Mitek A Johnson And Johnson recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2616-2017%22
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