Drug recall
Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
FDA recall event 93611 · Class II · Medtronic Navigation, Inc.
Key facts
| Event ID | 93611 |
|---|---|
| Recall numbers | Z-0698-2024, Z-0699-2024 |
| Recalling firm | Medtronic Navigation, Inc. |
| Product type | Devices |
| Products | Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS, Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove. |
| Initiation date | Nov 28, 2023 |
| Report date | Jan 17, 2024 |
| City | Lafayette |
| State | CO |
| Country | United States |
| FEI number | 1000517638 |
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: