ErgoSafe Products, LLC (DBA) Prism Medical recalls A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
- Recall date
- January 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1405-2017
- FDA classification
- Class II
- Brand / firm
- ErgoSafe Products, LLC (DBA) Prism Medical
- Sold / distributed
- Product was distributed to MT and NV; one VA consignee.
Why it was recalled
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Get recall alerts
Free email alert whenever ErgoSafe Products, LLC (DBA) Prism Medical has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: ErgoSafe Products, LLC (DBA) Prism Medical