Drug recall
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is…
FDA recall event 79518 · Class II · DePuy Mitek, Inc., a Johnson & Johnson Co.
Key facts
| Event ID | 79518 |
|---|---|
| Recall numbers | Z-1749-2018 |
| Recalling firm | DePuy Mitek, Inc., a Johnson & Johnson Co. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Reports of product loosening or coming unscrewed from the handle. |
| Initiation date | Dec 22, 2017 |
| Report date | May 16, 2018 |
| Termination date | Jul 16, 2019 |
| City | Raynham |
| State | MA |
| Country | United States |
| FEI number | 1221934 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: