The Recall Desk
HighFDA (Devices)·Z-1405-2017·Announced 2017-03-15

Prism Medical A625 Manual Lifts Recalled for Premature Strap Breakage

ErgoSafe Products is recalling 21 Prism Medical A625 manual lifts because two units had straps break prematurely during internal testing at maximum load.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (patient lift) where a structural failure (strap breakage) was identified during testing, but no injuries or illnesses have been reported to date.

Plain-English summary

ErgoSafe Products, LLC (DBA Prism Medical) is recalling 21 units of the A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni (Part No. 324124). The recall was initiated after internal cycle testing at the maximum load of 625 lbs. revealed that two units had straps that broke prematurely.

The affected products were distributed to Montana and Nevada, with one consignee located in Virginia. The recall covers specific serial codes listed in the agency record.

Consumers should stop using the affected lifts immediately and contact the recalling firm for instructions on repair or replacement.

The recalled product

Product
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Manufacturer
ErgoSafe Products, LLC (DBA) Prism Medical
Category
Medical Device — Patient Lifts
Hazard
Affected units
21

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 2 recalled by ErgoSafe Products, LLC (DBA) Prism Medical under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

Same manufacturer · ErgoSafe Products, LLC (DBA) Prism Medical

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Same hazard · structural failure

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