Drug recall
Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with…
FDA recall event 74656 · Class II · Richard Wolf Medical Instruments Corp.
Key facts
| Event ID | 74656 |
|---|---|
| Recall numbers | Z-2608-2016 |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Product type | Devices |
| Products | Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic accessories in gynecological laparoscopy, to determine patency of the fallopian… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The distal end of the Conical portio adapter (acorn) is composed of a small cap (head) that partially sits inside a hollow shaft (tube). These two parts are welded together to create one piece. In the… |
| Initiation date | May 19, 2016 |
| Report date | Aug 31, 2016 |
| Termination date | Nov 30, 2017 |
| City | Vernon Hills |
| State | IL |
| Country | United States |
| FEI number | 1418479 |
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: