Drug recall
Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated for either…
FDA recall event 69814 · Class II · Zimmer Manufacturing B.V.
Key facts
| Event ID | 69814 |
|---|---|
| Recall numbers | Z-0875-2015 |
| Recalling firm | Zimmer Manufacturing B.V. |
| Product type | Devices |
| Products | Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing primary or revision… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Zimmer received a single complaint wherein a Trilogy® Fiber Metal Multi-Hole Acetabular Shell would not attach to the inserter/impactor instrumentation. Subsequent investigation found the… |
| Initiation date | Dec 4, 2014 |
| Report date | Dec 31, 2014 |
| Termination date | Jun 18, 2015 |
| City | Mercedita |
| State | PR |
| Country | United States |
| FEI number | 1000132037 |
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: