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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Arjohuntleigh Magog: The spreader bar can detach from the scale attachment under certain conditions.

Agency Publication Date: August 7, 2018
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Affected Products

Product: Quick 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.

Product Code 700-19485: starting from serial number 300146551 up to serial number 300220716.

Lot Numbers:
700-19485
Product: 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.

Product Code 700-19490: starting from serial number 300142013 up to serial number 300219867.

Lot Numbers:
700-19490

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80465
Status: Resolved
Manufacturer: Arjohuntleigh Magog
Manufactured In: Canada
Units Affected: 2 products (874 Units (both styles))

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.