Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K914103 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator. | 2 | 04/06/2018 |
FEI # 1000086682 Lifeline Systems Company |
| Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System. | 2 | 10/01/2015 |
FEI # 1000086682 Lifeline Systems, Incorporated |
| Philips GoSafe Communicator 7000L Personal emergency response system. | 2 | 07/06/2015 |
FEI # 1000086682 Lifeline Systems, Incorporated |
| Philips Lifeline Personal Help Button Pendant Classic and Slimline Style. | 2 | 11/25/2009 |
FEI # 3007138625 Philips Lifeline Inc |
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