Drug recall
Stryker Orthopaedics Triathlon Tritanium Patella Inserter,. NON-STERILE Product Usage: The Triathlon…
FDA recall event 68500 · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Event ID | 68500 |
|---|---|
| Recall numbers | Z-1978-2014 |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Product type | Devices |
| Products | Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the Tritanium Knee System Instrument Set. It is used to… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Tritanium Patella Inserter Instrument fracture during implantation. . |
| Initiation date | May 1, 2014 |
| Report date | Jul 9, 2014 |
| Termination date | Jun 9, 2017 |
| City | Mahwah |
| State | NJ |
| Country | United States |
| FEI number | 3003070421 |
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: