Drug recall
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
FDA recall event 91160 · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Event ID | 91160 |
|---|---|
| Recall numbers | Z-0479-2023 |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Product type | Devices |
| Products | Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International) |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected. |
| Initiation date | Nov 11, 2022 |
| Report date | Dec 21, 2022 |
| 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: