Reported Dec 12, 2018 · Terminated

Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a Non-AC-Powered patient…

Invacare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Invacare Corporation · 1200 Taylor St · Elyria, OH · 44035-6248

Is this the product you have?

  • Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a Non-AC-Powered patient lift is to lift and transfer a patient from one surface to another, as from a bed to a wheelchair. The device includes straps and a sling to support the patient.
Lot codes and dates
  • Serial numbers ranging between 09FSZ590001 to 16ESZ104075. Specifically, serial numbers with the following starting values (see below). Each consignee will be receiving an impacted units list, which will include full serial numbers
  • for the units that they have purchased

    84 of 84 codes

    • 10ASZ
    • 11ASZ
    • 12ASZ
    • 13ASZ
    • 14ASZ
    • 15ASZ
    • 16ASZ
    • 10BSZ
    • 11BSZ
    • 12BSZ
    • 13BSZ
    • 14BSZ
    • 15BSZ
    • 16BSZ
    • 10CSZ
    • 11CSZ
    • 12CSZ
    • 13CSZ
    • 14CSZ
    • 15CSZ
    • 16CSZ
    • 10DSZ
    • 11DSZ
    • 12DSZ
    • 13DSZ
    • 14DSZ
    • 15DSZ
    • 16DSZ
    • 10ESSZ
    • 11ESSZ
    • 12ESSZ
    • 13ESSZ
    • 14ESSZ
    • 15ESSZ
    • 16ESSZ
    • 09FSZ
    • 10FSZ
    • 11FSZ
    • 12FSZ
    • 13FSZ
    • 14FSZ
    • 15FSZ
    • 09GSZ
    • 10GSZ
    • 11GSZ
    • 12GSZ
    • 13GSZ
    • 14GSZ
    • 15GSZ
    • 09HSZ
    • 10HSZ
    • 11HSZ
    • 12HSZ
    • 13HSZ
    • 14HSZ
    • 15HSZ
    • 09ISZ
    • 10ISZ
    • 11ISZ
    • 12ISZ
Amount recalled
73,703 units

Where it was sold

  • Nationwide

Why it was recalled

Invacare has identified via customer complaints, the potential for the mounting bolt connecting the caster to the base frame of the patient lifts to become loose. Loose hardware can cause wear to the hardware and housings. If left unresolved, the caster may separate from the base of the lift causing the Lift to tilt and a patient fall. Failure does not occur right away but happens over time if the lift is not properly maintained. Patient falls are inherently dangerous and may result in a range of injuries that are dependent on physical condition of the patient and the nature of the fall. When injuries occur, they are typically non-serious injuries such as bruising, lacerations, or abrasions. In rare cases, more serious injuries such as bone fracture, head trauma, or death can occur. For caregivers using the lift, attempts to manually stabilize a lift if it becomes unstable could result in sprains, serious back injuries, or bone fractures.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 15, 2020 · Data as of Sep 19, 6:52 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.