DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code:… — Class II medical device recall Z-2615-2017
Terminated recall by DePuy Mitek, Inc., a Johnson & Johnson Co., reported 2017-06-28, distributed in AZ, CA, CO, GA, MA, MI, OH, WA. Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being
| Recall number | Z-2615-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Mitek, Inc., a Johnson & Johnson Co., Raynham, MA, United States |
| Recall initiated | 2017-05-12 |
| Classified | 2017-06-20 |
| Reported by FDA | 2017-06-28 |
| Terminated | 2018-10-03 |
| Distributed | AZ, CA, CO, GA, MA, MI, OH, WA |
| Countries outside the US | AT, AU, BE, CH, DE, ES, FR, GB, NL, PL |
| Quantity | 173 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 10886705026890 |
| Lot numbers | 16D02, 16E01, 16J01, 17A01, 17B01, 17B02 |
Product
DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2615-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.