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

Recall Z-0065-2017 — TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

U.S. FDA — Device Enforcement · United States · 2016-06-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0065-2017
Date of alert: 2016-06-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Winco Mfg., LLC
Product category: device
Product type: Devices

Reported risk: Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0065-2017 — TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

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