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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 Likosee related information
Date Initiated by FirmSeptember 24, 2004
Date PostedJune 08, 2005
Recall Status1 Terminated 3 on June 20, 2007
Recall NumberZ-0876-05
Recall Event ID 31193
Product Classification Lift, Patient, Ac-Powered - Product Code FNG
ProductUNO 100 EM/EE Patient Lift
Code Information Serial Number: Range 7090602-7093161
Recalling Firm/
Manufacturer		 Liko, Inc.
842 Upper Union St., Suite 4
Franklin MA 02038
For Additional Information ContactJim Butler
888-545-6671
Manufacturer Reason
for Recall		Incorrect length support screws may cause patient lift failure
FDA Determined
Cause 2		Other
ActionLiko 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 Commerce398 units
DistributionCanada
Total Product Life CycleTPLC 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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