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All product recalls associated with RICON.
Total Recalls
134
Past Year
7
Class I (Serious)
0
Most Recent
Sep 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Ricon Corporation (Ricon) is recalling certain S-Series and K-Series Titanium Wheelchair Lifts, models K200, K201, K550, K551, S200, S2201, S550 and S551. The wheelchair lift positioning input cam may fail while the lift is in use, allowing the platform to travel higher than the vehicle's floor height. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 403, "Platform Lift Systems."
J-Tech Corporation (J-Tech) is recalling certain Icon Alliance Dark, Alliance GT Rubatone, and Alliance GT Horror motorcycle helmets in sizes XS, S, M, L, XL, XXL, and XXXL. The helmets may have faulty stitching on the webbing possibly allowing the D-rings to separate from the chin strap.
Dietary supplement contains excess amount of fluoride.
Ricon Corporation (Ricon) is recalling certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured August 26, 2014, to July 1, 2015. The platform side plate of the affected wheelchair lifts may crack. Additionally, the lifts are equipped with folding link arms that may have pivot holes that are too big, allowing the bearings to move out of position.
Gillig LLC (Gillig) is recalling certain Ricon Model S5510 Wheelchair lifts manufactured November 3, 2010, to February 25, 2011 and sold through the Gillig aftermarket parts department. The affected lifts are equipped with folding link arms that may have pivot holes that are too big, allowing the bearings to move out of position.
Ricon Corporation (Ricon) is recalling certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured January 1, 2006, to August 25, 2014. The affected lifts are equipped with folding link arms that may have pivot holes that are too big, allowing the bearings to move out of position.
Gillig LLC (Gillig) is recalling certain S5510 series wheelchair lifts sold as aftermarket accessory parts and manufactured by Ricon Corporation from November 30, 2010, to February 25, 2011. The platform side plate of the affected wheelchair lifts may crack.
Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black braid) meets the expected sterility assurance level for sterile products.
The device may have a non-conforming component that may cause the device to fire an unformed staple.
Ricon Corporation (Ricon) is recalling certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured after January 1, 2006. The platform side plate of the affected wheelchair lifts may crack.
Ricon Corporation is recalling certain S series and K series wheelchair lifts manufactured January 1, 2013, through January 4, 2014, and equipped with an optional armored pendant cable. The affected model numbers start with S2003, S2005, S2010, S5505, S5510, K2010, K5505, or K5510 and all of the model numbers end with a 'B' to denote being equipped with an armored pendant cord. The armored cable may be positioned such that it does not clear the wheelchair lift.
Ricon is recalling certain S series and K Series wheelchair lifts manufactured after August 1, 2006, and equipped with an optional armored pendant cable. The cable may have been installed such that it doesn't clear the wheelchair lift and without a protective cover, or a misinstalled protective cover.
Ricon is recalling the egress window handles of certain Ricon 3-Minute Urban Transit Bus egress window sets manufactured April 1, 2010, through October 31, 2010, sold and installed as original equipment for various transit buses. The composition of the material used to cast the handles is incorrect resulting in embrittlement of the handle and a reduction in material strength. The handle(s) on the emergency egress passenger windows may break before the window latch is released.
There is the potential for the duckbill seal to become dislodged.
The firm initiated this second subsequent recall because the affected devices can remain closed and clamped on tissue during surgical procedures due to the fact that the mechanism which connects the articulation joint to the device shaft is insufficient.
The firm initiated this second subsequent recall because the affected devices can remain closed and clamped on tissue during surgical procedures due to the fact that the mechanism which connects the articulation joint to the device shaft is insufficient.
Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process.
Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process.
Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process.
Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process.