Drug recall
US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible…
FDA recall event 82142 · Class II · US Endoscopy Group Inc
Key facts
| Event ID | 82142 |
|---|---|
| Recall numbers | Z-1011-2019 |
| Recalling firm | US Endoscopy Group Inc |
| Product type | Devices |
| Products | US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential esophageal laceration during a patient procedure |
| Initiation date | Feb 4, 2019 |
| Report date | Mar 20, 2019 |
| Termination date | Aug 3, 2020 |
| City | Mentor |
| State | OH |
| Country | United States |
| FEI number | 1000122656 |
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: