Drug recall
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system…
FDA recall event 63649 · Class II · Kimberly-Clark Corporation
Key facts
| Event ID | 63649 |
|---|---|
| Recall numbers | Z-0451-2013 |
| Recalling firm | Kimberly-Clark Corporation |
| Product type | Devices |
| Products | Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated for monitoring and controlling patient temperature. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately. |
| Initiation date | Sep 16, 2010 |
| Report date | Dec 5, 2012 |
| Termination date | Dec 20, 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: