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Terminated

UNO 100 Patient Lift

FDA Recall Z-0276-06 · Posted 2005-12-13

Recalling FirmLiko, Inc.
Recall StatusTerminated
Product CodeFSA
Date Initiated2005-11-14
Date Terminated2008-02-20
Product Quantity548 units

Reason for Recall

Incorrect length leg pin bolts may cause patient lift failures

Firm Action

Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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