Drug recall
Segmented Cervix Applicator Set, part number GM11004310, a component used with the tube for segments and…
FDA recall event 63667 · Class II · Varian Medical Systems, Inc.
Key facts
| Event ID | 63667 |
|---|---|
| Recall numbers | Z-0607-2013 |
| Recalling firm | Varian Medical Systems, Inc. |
| Product type | Devices |
| Products | Segmented Cervix Applicator Set, part number GM11004310, a component used with the tube for segments and cervical sleeves The guide tube for segments and cervical sleeves in the Segmented Cervix… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The guide tube which is part of the Segmented Cervix Applicator Set is difficult to disconnect from cervical sleeve. |
| Initiation date | Sep 28, 2012 |
| Report date | Dec 26, 2012 |
| Termination date | Apr 2, 2013 |
| City | Charlottesville |
| State | VA |
| Country | United States |
| FEI number | 3000206172 |
At a glance
- 1–9 Products in this recall
- 1–9 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: