Reported Mar 15, 2017 · Terminated
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and…
Physio-Control, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Physio-Control, Inc. · 11811 Willows Rd NE · Redmond, WA · 98052-2003
Is this the product you have?
- The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
- Lot codes and dates
- Affected Product Part Numbers
320371500XX. There are 133330 affected serial numbers
- Affected Product Part Numbers
- Amount recalled
- total 133,330 units (50,046 units in the US)
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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