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Terminated

A-series lift - A625 Manual Part No. 324117. Prism Medical.

FDA Recall Z-1406-2017 · Posted 2017-02-28

Recalling FirmErgoSafe Products, LLC (DBA) Prism Medical
Recall StatusTerminated
Product CodeFSA
Date Initiated2017-01-30
Date Terminated2017-12-04
Product Quantity76

Reason for Recall

During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

Firm Action

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

Distribution Pattern

Product was distributed to MT and NV; one VA consignee.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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