Drug recall
Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a…
FDA recall event 67648 · Class II · Teleflex Medical
Key facts
| Event ID | 67648 |
|---|---|
| Recall numbers | Z-1506-2014 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a gastrointestinal tube and accessories, consisting of flexible or semi-rigid tubing used for… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Sterility of the product cannot be guaranteed. |
| Initiation date | Mar 4, 2014 |
| Report date | Apr 30, 2014 |
| Termination date | Jan 28, 2016 |
| City | Durham |
| State | NC |
| Country | United States |
| FEI number | 3005747797 |
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: