Drug recall
Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift…
FDA recall event 70151 · Class II · Penner Mfg Inc
Key facts
| Event ID | 70151 |
|---|---|
| Recall numbers | Z-1306-2015 |
| Recalling firm | Penner Mfg Inc |
| Product type | Devices |
| Products | Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and injury to the operator or patient could result. The device manual was updated with an… |
| Initiation date | Jan 30, 2015 |
| Report date | Apr 1, 2015 |
| Termination date | Mar 10, 2016 |
| City | Aurora |
| State | NE |
| Country | United States |
| FEI number | 1922538 |
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: