Liko Universal Sling Bar 450 R2R Product NUmber: 3156095
FDA Recall Z-1118-2007 · Posted 2007-07-23
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Recalling FirmLiko, Inc.
Recall StatusTerminated
Product CodeFRW
Date Initiated2007-06-13
Date Terminated2015-10-20
Product Quantity3 units
Reason for Recall
Sling bar may have a center bolt break at the adapter while in use
Firm Action
Liko Inc notified distributors and end users by letter on 6/13/07.
Root Cause
Component design/selection
Distribution Pattern
Nationwide
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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