CPSCMarch 20, 2012consumer
Bon Hiver Recalls Freebase Snowboard Bindings Due To Fall Hazard
Official recall recorded by the U.S. Consumer Product Safety Commission.
The hazard
The binding's base plate can fracture from impact during use, posing a fall hazard to snowboarders.
What to do
Consumers should immediately stop using the recalled bindings and return them to Bon Hiver for a free repair and a 20 percent refund of the purchase price.
Brands named
bon hiversnowboardsnowboard bindingsbon
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDABrand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction w...2026-04-16
- FDAFreelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S2021-10-15
- FDAFREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas c Systems, REF: LK016.CB, IVD CE, UDI: 050517000120962021-05-20
- FDAOptilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A2020-11-18
- FDAThe Optilite Clinical Chemistry Analyzer. IVD. Model Number: IE700. UDI-05051700017176 - Product Usage: The Optilite Clinical Chemistry Analyzer is a fully automated random access analyzer used to measure a variety of analytes that may be adaptable to the analyzer depending on the reagent used.2020-04-09
- FDARheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI: 050517000183192019-11-06
- FDAOptilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: 05051700020015 (kit ea. containing four components)2019-10-07
- FDAOPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 050517000175652019-07-29
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