Medibo Minerva Patient Lift

Modified on 2009/10/14 21:40 by admin
In September 2004, the FDA and Medibo notified healthcare professionals of a Class I recall of the Minerva patient lift (models ML-20 and ML-30). The Minerva patient lift is intended to be used to raise and transport patients from one location to another, such as from a bed to a bath.

There are three mechanical problems for which the Minerva patient lift is currently being recalled. The first involves the hanger bar detaching from the lift resulting in the patient falling to the ground because of a missing spring washer. The second problem involves a bolt in the foot pedal assembly becoming loose which allows the foot pedal assembly to fall off of the lift. This results in the lift becoming unstable and the patient possibly falling. Thirdly, some units may have faulty actuator brackets on the mast assembly that can also cause the lift to become unstable.

Class I recalls are the most serious type of recall and involve situations where there is a reasonable probability that use of the product will cause serious injury or death.

If you have been injured because of a defective patient lift, it may be important to contact an attorney who can help you protect your legal rights. Please keep in mind that there may be time limits within which you must commence suit.

*Source: Food and Drug Administration

See Also

  1. Defective & Dangerous Products: Overview
  2. Broken Back: Overview
  3. Broken Bones: Overview
  4. Dislocation: Overview
  5. Joints & Muscles: Overview
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