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

Recall Z-2661-2018 — Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospitals, nursing homes, home care or health care facilities.

U.S. FDA — Device Enforcement · Canada · 2018-02-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2661-2018
Date of alert
2018-02-12
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Arjohuntleigh Magog
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
300142013
Reported risk: The spreader bar can detach from the scale attachment under certain conditions.
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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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.