Drug recall
SlingBar 350. Designed to meet the needs for lifting humans.
FDA recall event 64550 · Class II · Hill-Rom, Inc.
Key facts
| Event ID | 64550 |
|---|---|
| Recall numbers | Z-1473-2013, Z-1474-2013, Z-1475-2013, Z-1476-2013 |
| Recalling firm | Hill-Rom, Inc. |
| Product type | Devices |
| Products | SlingBar 350. Designed to meet the needs for lifting humans., SlingBar 360. Designed to meet the needs for lifting humans., SlingBar Standard. Designed to meet the needs for lifting humans., SlingBar Wide 670. Designed to meet the needs for lifting humans. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to… |
| Initiation date | Apr 30, 2013 |
| Report date | Jun 12, 2013 |
| Termination date | Nov 28, 2014 |
| City | Batesville |
| State | IN |
| Country | United States |
| FEI number | 1824206 |
At a glance
- 1–9 Products in this recall
- 10–99 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: