Stanley M200 Fall Monitoring System Recall: Damaged Capacitor Risk
Stanley Security Solutions recalls M200 Fall Monitoring Systems with damaged capacitors. Serial numbers 68015-73369 listed. Stop using immediately to prevent potential electrical hazards.
Recall notice
Damaged capacitor on the printed circuit board.
Contact the company
What happened, in plain English
Stanley Security Solutions is recalling M200 Fall Monitoring Systems with damaged capacitors. This issue could cause electrical problems if the device is used, so it's important to stop using these units immediately. Read more at govinfonow.com/recall/69641-stanley-m200-fall-monitoring-system-recall-damaged-capacitor-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/69641-stanley-m200-fall-monitoring-system-recall-damaged-capacitor-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1349-2019
Cite this page
“Stanley M200 Fall Monitoring System Recall: Damaged Capacitor Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/69641-stanley-m200-fall-monitoring-system-recall-damaged-capacitor-risk. Based on FDA recall #Z-1349-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1349-2019%22&limit=1).
Why it’s dangerous
The device has a damaged capacitor on the printed circuit board, which can lead to electrical issues. However, the recall record does not specify what kind of electrical problem or how severe it could be.
Who’s affected
Owners of M200 Fall Monitoring Systems with serial numbers listed from 68015 to 73369 are affected. People who use these devices for fall monitoring in homes or workplaces are most at risk.
How to tell if you have this one
Check the serial number on your M200 Fall Monitoring System. The affected units have serial numbers starting with 68015 and ending with 73369 as listed in the recall.
- Brand
Stanley Security Solutions- Category
Medical device
What to do — step by step
Stop Using Immediately
The recall states that the device has a damaged capacitor, so stop using it right away to avoid potential electrical hazards.
Where it went and when
Where it was distributed
Distributed in 7 states, and outside the U.S.
FDA distribution: “CT, FL, OH, OK, TX, WA, and WV Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, Florida, Ohio, Oklahoma, Texas, Washington, West Virginia.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1349-2019 (October 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1349-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.