Drug recall
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
FDA recall event 79886 · Class II · Richard Wolf GmbH
Key facts
| Event ID | 79886 |
|---|---|
| Recall numbers | Z-1868-2018 |
| Recalling firm | Richard Wolf GmbH |
| Product type | Devices |
| Products | RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Tube ends may be mixed up. |
| Initiation date | Mar 11, 2018 |
| Report date | May 23, 2018 |
| Termination date | Mar 9, 2022 |
| City | Knittlingen |
| Country | Germany |
| FEI number | 3002808001 |
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: