Lifeline Systems, Incorporated recalls Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
- Recall date
- July 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0004-2016
- FDA classification
- Class II
- Brand / firm
- Lifeline Systems, Incorporated
- Sold / distributed
- Nationwide Distribution -- AK, AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, MA, MD, MI, MN, MT, NC, NE, NJ, NY, OH, OK, OR, PA, SC, TX, UT, VA, VT, WA, and WI.
Why it was recalled
Irregular battery disconnection resulted in issues with Mobile Health Button (MHB) Charging.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
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