Drug recall
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical…
FDA recall event 72273 · Class II · Berchtold Corp.
Key facts
| Event ID | 72273 |
|---|---|
| Recall numbers | Z-0154-2016 |
| Recalling firm | Berchtold Corp. |
| Product type | Devices |
| Products | TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the control board assembly. |
| Initiation date | Sep 23, 2015 |
| Report date | Oct 28, 2015 |
| Termination date | Nov 17, 2016 |
| City | 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: