Drug recall
Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx Only, Sterile, REF 543965 Product…
FDA recall event 73181 · Class II · Teleflex Medical
Key facts
| Event ID | 73181 |
|---|---|
| Recall numbers | Z-0886-2016 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx Only, Sterile, REF 543965 Product Usage: The Weck Auto Endo5 hem-o-lok ML automatic endoscopic ligating clip appliers are… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The clip in the applier may be missing a boss. A boss is the part of the clip that is used to hold the clip within the applier jaws prior to application. |
| Initiation date | Feb 2, 2016 |
| Report date | Mar 2, 2016 |
| Termination date | Aug 11, 2017 |
| City | Research Triangle Park |
| State | NC |
| Country | United States |
| FEI number | 1044475 |
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: