LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet… — Class II medical device recall Z-1749-2018
Terminated recall by DePuy Mitek, Inc., a Johnson & Johnson Co., reported 2018-05-16, distributed nationwide. Reports of product loosening or coming unscrewed from the handle.
| Recall number | Z-1749-2018 |
|---|---|
| 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 | 2017-12-22 |
| Classified | 2018-05-08 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2019-07-16 |
| Distributed | Nationwide (US) |
| Quantity | 84 |
Product
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries.
Reason for recall
Reports of product loosening or coming unscrewed from the handle.
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-1749-2018. 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.