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Terminated

UNO 102 EM/EE/ES Patient Lift

FDA Recall Z-0875-05 · Posted 2005-06-08

Recalling FirmLiko, Inc.
Recall StatusTerminated
Product CodeFNG
Date Initiated2004-09-24
Date Terminated2007-06-20
Product Quantity21 units

Reason for Recall

Incorrect length support screws may cause patient lift failure

Firm Action

Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.

Root Cause

Other

Distribution Pattern

Canada

Official Source

View FDA Recall →

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

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