Drug recall
Arthrex Suture Washer
FDA recall event 75050 · Class III · Arthrex, Inc.
Key facts
| Event ID | 75050 |
|---|---|
| Recall numbers | Z-2918-2016 |
| Recalling firm | Arthrex, Inc. |
| Product type | Devices |
| Products | Arthrex Suture Washer |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package. |
| Initiation date | Aug 12, 2016 |
| Report date | Oct 12, 2016 |
| Termination date | Aug 20, 2019 |
| City | Naples |
| State | FL |
| Country | United States |
| FEI number | 1220246 |
At a glance
- 1–9 Products in this recall
- 10–99 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: