Sabina I and II EM/EE Patient Lift
FDA Recall Z-0877-05 · Posted 2005-06-08
Recalling FirmLiko, Inc.
Recall StatusTerminated
Product CodeFNG
Date Initiated2004-09-24
Date Terminated2007-06-20
Product Quantity531 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.