Drug recall
Kimberly Clark Patient Warming System - Model 1000 Control Unit. Kimberly Clark Patient Warming System - Model…
FDA recall event 62596 · Class II · Kimberly-Clark Corporation
Key facts
| Event ID | 62596 |
|---|---|
| Recall numbers | Z-2181-2012 |
| Recalling firm | Kimberly-Clark Corporation |
| Product type | Devices |
| Products | Kimberly Clark Patient Warming System - Model 1000 Control Unit. Kimberly Clark Patient Warming System - Model 1000 Control Unit and Energy Transfer Pads is a thermal regulating system, indicated for… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A defect of the "fuse holder" can lead to a Control Unit failure that may cause the device to lose its ability to warm and maintain set temperature and may also result in excessive heat with the fuse… |
| Initiation date | Apr 27, 2012 |
| Report date | Aug 15, 2012 |
| Termination date | Sep 5, 2012 |
| City | Roswell |
| State | GA |
| Country | United States |
| FEI number | 1000015879 |
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: