ARJOHUNTLEIGH POLSKA Sp. z.o.o.: Medical Device Recall in 2022 - (Recall #: Z-1098-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Sara Plus Active Floor Lift

Product Classification:

Class I

Date Initiated: April 5, 2022

Date Posted: June 1, 2022

Recall Number: Z-1098-2022

Event ID: 89960

Reason for Recall:

The device may emit smoke or ignite.

Status: Terminated

Product Quantity: 4449 devices

Code Information:

Model 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

Distribution Pattern:

US Nationwide and Worldwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated