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.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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
- Affected units
- 21
Distribution
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
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