FDA recall Z-1205-2023

Med-Mizer, Inc. · Class II · device

Product

Sit to Stand STS500 Patient Lift

Reason for recall

Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.

Distribution

Awaiting consignee list from the recalling firm.

Key facts

Status
Ongoing
Initiation date
2023-02-03
Report date
2023-03-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Batesville, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1205-2023