Drug recall
Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane protector; this is placed inside…
FDA recall event 62764 · Class II · DePuy Orthopaedics, Inc.
Key facts
| Event ID | 62764 |
|---|---|
| Recall numbers | Z-0569-2013 |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Product type | Devices |
| Products | Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane protector; this is placed inside an uncoated Tyvek/PET peel pouch and sealed. This package is placed into a paperboard… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the Pinnacle¿ Cancellous Screw due to an incorrect description on the label. The label description reads Pinnacle Cannulated Screw… |
| Initiation date | Nov 28, 2012 |
| Report date | Dec 26, 2012 |
| Termination date | Mar 20, 2013 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1818910 |
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: