FDA Device recall Z-1254-2022
MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to commu…
- FDA Device
- Class II
- terminated
- Published 2022-06-15
On 2022-06-15 the FDA classified a Class II recall of MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to commu… by Medminder Systems, citing discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feat….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1254-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-03-28 |
| Published | 2022-06-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medminder Systems |
| Distribution | US |
Product
MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.
Reason
Discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feature(button) removed
Identifiers
| code_info | Serial Numbers: mm30335 mm28673 mm30365 mm30151 mm80451 mm80219 mm27838 mm80203 mm80607 mm27353 mm30922 mm30177 mm27576…Serial Numbers: mm30335 mm28673 mm30365 mm30151 mm80451 mm80219 mm27838 mm80203 mm80607 mm27353 mm30922 mm30177 mm27576 mm30027 mm27584 mm80550 mm80224 mm80109 mm30320 mm28129 mm27317 mm28656 mm27824 mm80584 mm28569 mm30458 mm28220 mm30285 mm80748 mm30765 mm30673 mm30703 mm27386 mm30836 mm30893 mm80496 mm30099 mm80338 mm80067 mm80282 mm30692 mm27156 mm30198 mm28702 mm30945 mm27899 mm30821 mm27631 mm31006 mm27729 mm27635 mm28107 mm80056 mm30160 mm30457 mm30656 mm28077 mm27293 mm28670 mm27049 mm80535 mm27517 mm80317 mm30319 mm30256 mm27132 mm80312 mm28175 mm27987 mm30626 mm30607 mm27369 mm27001 mm30304 mm30602 mm80264 mm28067 mm30909 mm30643 mm30541 mm30824 mm30115 mm30328 mm30341 mm30521 mm30100 mm80381 mm30844 mm30293 mm30654 mm28232 mm80290 mm80527 mm27272 mm30251 mm80423 mm30376 mm27446 mm80083 mm27853 mm30484 mm27301 mm80726 mm80627 mm30230 mm27352 mm27217 mm30127 mm80010 mm30142 mm80196 mm30715 mm30663 mm27082 mm27278 mm30128 mm27796 mm28170 mm30923 mm80418 mm80521 mm30725 mm27579 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1254-2022%22
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