Drug recall
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled…
FDA recall event 92499 · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Event ID | 92499 |
|---|---|
| Recall numbers | Z-2130-2023 |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Product type | Devices |
| Products | Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or… |
| Initiation date | May 24, 2023 |
| Report date | Jul 19, 2023 |
| 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: