Sara Plus Active Floor Lift — FDA record Z-1098-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 5, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Sara Plus Active Floor Lift
Reason
The device may emit smoke or ignite.
Classification
Class I
Recalling firm
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Quantity
4449 devices
Agency-reported status
Terminated
Source record identifier
Z-1098-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityModel Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide and Worldwide distribution

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jun 1, 2022
Recall initiation date
Apr 5, 2022
Center classification date
May 20, 2022
Termination date
Sep 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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