Drug recall
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
FDA recall event 68470 · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Event ID | 68470 |
|---|---|
| Recall numbers | Z-2122-2014 |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Product type | Devices |
| Products | InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stryker has received complaints from the field alleging instances where the In Touch beds are hoisted or lifted from the floor and the casters have fallen off. The investigations into these casters… |
| Initiation date | Jun 4, 2014 |
| Report date | Aug 6, 2014 |
| Termination date | Mar 14, 2016 |
| City | Portage |
| State | MI |
| Country | United States |
| FEI number | 1831750 |
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: