Drug recall
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product…
FDA recall event 83108 · Class III · CooperSurgical, Inc.
Key facts
| Event ID | 83108 |
|---|---|
| Recall numbers | Z-0029-2020 |
| Recalling firm | CooperSurgical, Inc. |
| Product type | Devices |
| Products | Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The touchpad may not work properly after cleaning. |
| Initiation date | Sep 5, 2019 |
| Report date | Oct 9, 2019 |
| Termination date | Sep 2, 2021 |
| City | Trumbull |
| State | CT |
| Country | United States |
| FEI number | 1216677 |
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: