Drug recall
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
FDA recall event 78839 · Class II · Medtronic Sofamor Danek USA Inc
Key facts
| Event ID | 78839 |
|---|---|
| Recall numbers | Z-0566-2018 |
| Recalling firm | Medtronic Sofamor Danek USA Inc |
| Product type | Devices |
| Products | Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification. |
| Initiation date | Dec 22, 2017 |
| Report date | Feb 21, 2018 |
| Termination date | Jul 31, 2018 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 1000477302 |
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: