Drug recall
Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures.
FDA recall event 62683 · Class III · Berchtold Corp.
Key facts
| Event ID | 62683 |
|---|---|
| Recall numbers | Z-2148-2012 |
| Recalling firm | Berchtold Corp. |
| Product type | Devices |
| Products | Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defective camera: There is a possibility that the connection of the wires to the connector may become loose, causing image distortion or loss. |
| Initiation date | Jul 10, 2012 |
| Report date | Aug 15, 2012 |
| Termination date | Jun 6, 2013 |
| City | N Charleston |
| State | SC |
| Country | United States |
| FEI number | 1220685 |
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: