Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Lifeline Systems with 4 510(k) clearances and 3 device recalls. The most recent is a device recall dated Nov 13, 2017: HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator..
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 13, 2017 | HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator.Class II · A programing error in some Model FD100 HomeSafe AutoAlert Pendants will render the fall detection feature inoperable. | Device recalls |
| Dec 1, 2010 | M3810A PHILIPS TELEMONITORING SYSTEM WITH EDEVICE BRIDGED130K103214 · DRG | 510(k) clearances |
| Sep 27, 1991 | LIFELINE(R) PERSONAL RESPONSE SYSTEMK914103 · ILQ | 510(k) clearances |
| May 21, 1984 | BLOOD PRESSURE MONITOR BP600XK834441 · DXN | 510(k) clearances |
| Nov 14, 1983 | SINGLE BED ARRHYTHMIA MONITOR AM500K831638 · DSI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
