FDA Device recall Z-0004-2016
Philips GoSafe Mobile Help Button
- FDA Device
- Class II
- terminated
- Published 2015-10-07
On 2015-10-07 the FDA classified a Class II recall of Philips GoSafe Mobile Help Button by Lifeline Systems, citing irregular battery disconnection resulted in issues with Mobile Health Button (MHB) Charging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0004-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-23 |
| Published | 2015-10-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Lifeline Systems |
| Distribution | US |
Product
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Reason
Irregular battery disconnection resulted in issues with Mobile Health Button (MHB) Charging.
Identifiers
| code_info | Serial Numbers: 1030000887 1030000931 1030000934 1030000993 1030001039 1030001057 1030001059 1030001173 1030001…Serial Numbers: 1030000887 1030000931 1030000934 1030000993 1030001039 1030001057 1030001059 1030001173 1030001182 1030001210 1030001226 1030001254 1030001292 1030001315 1030001318 1030001358 1030001371 1030001441 1030001460 1030001526 1030001528 1030001568 1030001640 1030001641 1030001710 1030001720 1030001743 1030001797 1030001807 1030001819 1030002013 1030002025 1030002051 1030002129 1030002185 1030002214 1030002225 1030002233 1030002252 1030002316 1030002331 1030002406 1030002413 1030002444 1030002458 1030002489 1030002524 1030002534 1030002582 1030002601 1030002622 1030002626 1030002638 1030002669 1030002673 1030002689 1030002690 1030002715 1030002736 1030002755 1030002764 1030002881 1030002886 1030002889 1030002890 1030002904 1030002905 1030002924 1030002942 1030002946 1030002947 1030002969 1030002975 1030003005 1030003013 1030003015 1030003044 1030003077 1030003098 1030003143 1030003186 1030003284 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0004-2016%22
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