Med-Mizer, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1205-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Sit to Stand STS500 Patient Lift

Product Classification:

Class II

Date Initiated: February 3, 2023

Date Posted: March 8, 2023

Recall Number: Z-1205-2023

Event ID: 91695

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.

Status: Ongoing

Product Quantity: 37 units

Code Information:

UDI-DI: 00852195007353; Serial No.: STS500000, STS500001, STS500002, STS500003, STS500004, STS500005, STS500006, STS500007, STS500008, STS500009, STS500010, STS500011, STS500012, STS500013, STS500014, STS500015, STS500016, STS500017, STS500018, STS500019, STS500020, STS500021, STS500022, STS500023, STS500024, STS500025, STS500026, STS500027, STS500028, STS500029, STS500030, STS500031, STS500032, STS500033, STS500034, STS500035, and STS500036.

Distribution Pattern:

Awaiting consignee list from the recalling firm.

Voluntary or Mandated:

Voluntary: Firm initiated