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U.S. Department of Health and Human Services

Class 2 Device Recall Liko Universal Sling Bar

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 Class 2 Device Recall Liko Universal Sling Barsee related information
Date Initiated by FirmJune 13, 2007
Date PostedJuly 23, 2007
Recall Status1 Terminated 3 on October 20, 2015
Recall NumberZ-1117-2007
Recall Event ID 38194
Product Classification Sling Bar - Product Code FRW
ProductLiko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085
Code Information Serial Numbers: 1200101 through 1201281
FEI Number 3001451524
Recalling Firm/
Manufacturer		 Liko, Inc.
122 Grove Street
Suite 201
Franklin MA 02038
For Additional Information ContactAnne Jordan
508-553-3993
Manufacturer Reason
for Recall		Sling bar may have a center bolt break at the adapter while in use
FDA Determined
Cause 2		Component design/selection
ActionLiko Inc notified distributors and end users by letter on 6/13/07.
Quantity in Commerce22
DistributionNationwide
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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