A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
FDA device recall Z-1405-2017 · posted 2017-02-28 · Terminated
Recall details
- Recalling firm
- ErgoSafe Products, LLC (DBA) Prism Medical
- Reason for recall
- During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
- Action taken
- The recalling firm called each customer on Jan 30, 2017 to review the recall and schedule a time for the firm to come to their facility to personally swap the recalled product for a new device. The FSNs were sent on Jan 31, 2017.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FSA
- Quantity affected
- 21
- Distribution
- Product was distributed to MT and NV; one VA consignee.
- Date initiated
- 2017-01-30
- Date posted
- 2017-02-28
- Date terminated
- 2017-12-04
- Location
- Maryland Heights, MO
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