Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0877-05

Sabina I and II EM/EE Patient Lift

Liko, Inc. / initiated 2004-09-24 / Terminated

Liko, Inc. began a recall of Sabina I and II EM/EE Patient Lift on . The reason FDA records is "Incorrect length support screws may cause patient lift failure". As of , the recall status on record is Terminated.

Recall record

Recall number
Z-0877-05
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Liko, Inc.
Product
Sabina I and II EM/EE Patient Lift
Product code
FNG Lift, Patient, Ac-Powered
Reason for recall
Incorrect length support screws may cause patient lift failure
FDA root cause
Other
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.
Quantity in commerce
531 units
Distribution
Canada
Product codes and lots
Serial Number: Range 401205-41442