CLASS II Device recall · Reported 15 Mar 2017 · FDA Enforcement Report
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni recalled
ErgoSafe Products LLC ( is recalling A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni, distributed in Montana, Nevada, Virginia. The recall was initiated on 30 Jan 2017 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1405-2017
- FDA event ID
- 76351
- Recalling firm
- ErgoSafe Products LLC (, Maryland Heights, MO
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Jan 2017
- FDA classified
- 3 Mar 2017
- Reported
- 15 Mar 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 30 Jan 2017 | Recall initiated by company | |
| 3 Mar 2017 | Classified by FDA | +32 days |
| 15 Mar 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Where it was distributed
Product was distributed to MT and NV; one VA consignee.
Questions about this recall
Why was it recalled?
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Which lots are affected?
A6MC000110 A6M0001010 A6M0001011 A6M0001012 A6M0001013 A6M0001014 A6M0001015 A6M0001016 A6M0001017 A6M0001018 A6M0001019 A6M0001020 A6M0001021 A6M0001025 A6M0001026 A6M0001029 A6M0001022 A6M0001023 A6M0001024 A6M0001027 A6M0001028
Where was it sold?
Product was distributed to MT and NV; one VA consignee.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 76351This product is part of a recall event; the main page for the event is A-series lift - A625 Manual recalled by ErgoSafe Products, LLC (.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | A-series lift - A625 Manual recalled by ErgoSafe Products, LLC ( | ErgoSafe Products LLC ( | Device Malfunction | MT, NV, VA |
More recalls from ErgoSafe Products LLC (
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | A-series lift - A625 Manual recalled by ErgoSafe Products, LLC ( | ErgoSafe Products LLC ( | Device Malfunction | MT, NV, VA |
| Device | CLASS II | Carry bar which is an accessory to a lift used recalled | ErgoSafe Products LLC ( | Foreign Material | Nationwide |
| Device | CLASS II | Prism Medical C-300 Consumer Ceiling Lift recalled | ErgoSafe Products LLC ( | Other | Nationwide |
| Device | CLASS II | Prism Medical P-300 Portable Consumer Lift recalled | ErgoSafe Products LLC ( | Other | Nationwide |
| Device | CLASS II | Prism Medical P-600 Portable Ceiling Lift recalled | ErgoSafe Products LLC ( | Device Malfunction | Nationwide |
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