FDA recall record

Stryker Medical Division of Stryker Power-LOAD Cot Fastening System, Model #6390, Catalog recall — FDA Z-1389-2018

The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.

Class IIclassification
Z-1389-2018official record ID
Apr 25, 2018report date

Recall record at a glance

Official recordZ-1389-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Medical Division of Stryker Corporation
Report dateApr 25, 2018
Recall initiation dateMar 12, 2018
Quantity4724
LocationPortage, MI, United States

Official product description

Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and unloading of a compatible wheeled stretcher (ambulance cot) to and from a transport vehicle and to secure the ambulance cot during transport. The device has a maximum safe working load of 870 lb (395 kg), which includes the weight of the ambulance cot, patient, and equipment attached to the cot (such as oxygen bottles, monitors, and pumps). The intended users of the device are trained professionals, including emergency medical service and medical care center personnel, as well as medical first responders, service technicians and installers.

Why the product was recalled

The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.

Distribution information

Worldwide Distribution - USA (nationwide) and to the countries of : Australia, Canada, France, Germany, Hong Kong, Italy, India, Netherlands, Portugal, Saint Martin, Switzerland, United Kingdom

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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