Drug recall
E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology
FDA recall event 64927 · Class II · Kreg Medical Inc.
Key facts
| Event ID | 64927 |
|---|---|
| Recall numbers | Z-1480-2013 |
| Recalling firm | Kreg Medical Inc. |
| Product type | Devices |
| Products | E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position. |
| Initiation date | Aug 2, 2012 |
| Report date | Jun 12, 2013 |
| Termination date | Mar 2, 2018 |
| City | Chicago |
| State | IL |
| Country | United States |
| FEI number | 3005179379 |
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: