MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence…
Medical device recall Z-1254-2022. Published in FDA’s Enforcement Report on Jun 15, 2022.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jun 15, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 2701 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.
2701 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 2,000 characters
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 mm30803 mm80747 mm80328 mm80695 mm80618 mm80188 mm30790 mm80474 mm80561 mm80214 mm30943 mm30914 mm28674 mm30898 mm80325 mm30859 mm80583 mm28195 mm28713 mm27183 mm80183 mm28662 mm80733 mm80580 mm30275 mm27711 mm28503 mm30156 mm80537 mm28709 mm30139 mm30030 mm27324 mm30213 mm30012 mm30265 mm27815 mm27508 mm28649 mm27642 mm80684 mm27084 mm27512 mm80220 mm30834 mm30494 mm27964 mm30243 mm28672 mm27286 mm30361 mm27975 mm27998 mm80740 mm28585 mm28573 mm30162 mm28028 mm27604 mm30674 mm30167 mm80161 mm30339 mm27018 mm80692 mm30105 mm28093 mm28688 mm28562 mm30737 mm30699 mm27048 mm30757 mm27403 mm30976 mm30730 mm30244 mm27135 mm30763 mm80522 mm30854 mm80036 mm30606 mm30784 mm28186 mm30067 mm27368 mm80198 mm80656 mm30612 mm28556 mm80601 mm27535 mm80033 mm30848 mm28197 mm80622 mm80678 mm30165 mm30975 mm31035 mm30644 mm30331 mm80058 mm27414 mm80689 mm80045 mm80189 mm30796 mm28151 mm30045 mm80111 mm27734 mm27657 mm27194 mm27190 mm30677 mm30684 mm27839 mm80099 mm30885 mm30362 mm80126 mm80257 mm80374…
FDA’s list runs to 22,066 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Nationwide
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Mar 28, 2022.
- FDA classified it on Jun 9, 2022.
- FDA’s Enforcement Report published it on Jun 15, 2022.
- FDA terminated it on Jan 19, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Medminder Systems, Inc., of Needham, MA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 22,066 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.