AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Reported: December 27, 2023 Initiated: November 6, 2023 #Z-0567-2024
Product Description
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Reason for Recall
AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.
Details
- Recalling Firm
- Physio-Control, Inc.
- Units Affected
- 18,732
- Distribution
- US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.
- Location
- Redmond, WA
Frequently Asked Questions
What product was recalled? ▼
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098. Recalled by Physio-Control, Inc.. Units affected: 18,732.
Why was this product recalled? ▼
AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 27, 2023. Severity: Moderate. Recall number: Z-0567-2024.
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