Data Foundry

Medical device recalls 2019

M200 Fall Monitoring System — Class II medical device recall Z-1349-2019

Terminated recall by Stanley Security Solutions Inc, reported 2019-05-22, distributed in CT, FL, OH, OK, TX, WA, WV. Damaged capacitor on the printed circuit board.

Recall numberZ-1349-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStanley Security Solutions Inc, Lincoln, NE, United States
Recall initiated2018-10-11
Classified2019-05-15
Reported by FDA2019-05-22
Terminated2020-04-10
DistributedCT, FL, OH, OK, TX, WA, WV
Countries outside the USCA
Quantity1,101
Serial numbers68015, 68016, 68017, 68018, 68019, 68020, 68021, 68022, 68023, 68024, 68025, 68026, 68027, 68028, 68029, 68030, 68031, 68032, 68033, 68034, 68035, 68036, 68037, 68038, 68039 and 475 more

Product

M200 Fall Monitoring System

Reason for recall

Damaged capacitor on the printed circuit board.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1349-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.