Drug recall
The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor…
FDA recall event 75743 · Class II · Physio-Control, Inc.
Key facts
| Event ID | 75743 |
|---|---|
| Recall numbers | Z-0761-2017 |
| Recalling firm | Physio-Control, Inc. |
| Product type | Devices |
| Products | The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings within the environmental conditions specified. Product Part Numbers… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Customer complaint was received relating to a LifePak15 device that would power on then power down unexpectedly after a short period of use. When the LP15 powered down, power could be immediately… |
| Initiation date | Mar 11, 2010 |
| Report date | Dec 21, 2016 |
| Termination date | Dec 16, 2016 |
| City | Redmond |
| State | WA |
| Country | United States |
| FEI number | 3015876 |
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: