Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0587-2016 — MOVES System Lithium Polymer Batteries The MOVES System is a portable computer controlled electrically powered transport emergency ventilator intended to provide continuous or intermittent ventilatory support for the care of adults who require ventilation.

U.S. FDA — Device Enforcement · Canada · 2015-11-19 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0587-2016
Date of alert
2015-11-19
Country / jurisdiction
Canada
Risk level
Class I
Risk type
recall
Brand
Thornhill Research Inc
Product category
device
Product type
Devices
Reported risk: Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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