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U.S. Department of Health and Human Services

Class 2 Device Recall Liko

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  Class 2 Device Recall Liko see related information
Date Initiated by Firm September 24, 2004
Date Posted June 08, 2005
Recall Status1 Terminated 3 on June 20, 2007
Recall Number Z-0875-05
Recall Event ID 31193
Product Classification Lift, Patient, Ac-Powered - Product Code FNG
Product UNO 102 EM/EE/ES Patient Lift
Code Information Serial Numbers: Range 33590-42291
Recalling Firm/
Manufacturer		 Liko, Inc.
842 Upper Union St., Suite 4
Franklin MA 02038
For Additional Information Contact Jim Butler
888-545-6671
Manufacturer Reason
for Recall		 Incorrect length support screws may cause patient lift failure
FDA Determined
Cause 2		 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 21 units
Distribution Canada
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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