ErgoSafe Products, LLC (DBA) Prism Medical: Medical Device Recall in 2017 - (Recall #: Z-1405-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.

Product Classification:

Class II

Date Initiated: January 30, 2017

Date Posted: March 15, 2017

Recall Number: Z-1405-2017

Event ID: 76351

Reason for Recall:

During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

Status: Terminated

Product Quantity: 21

Code Information:

A6MC000110 A6M0001010 A6M0001011 A6M0001012 A6M0001013 A6M0001014 A6M0001015 A6M0001016 A6M0001017 A6M0001018 A6M0001019 A6M0001020 A6M0001021 A6M0001025 A6M0001026 A6M0001029 A6M0001022 A6M0001023 A6M0001024 A6M0001027 A6M0001028

Distribution Pattern:

Product was distributed to MT and NV; one VA consignee.

Voluntary or Mandated:

Voluntary: Firm initiated