Tip-over and fall hazard recalls
Furniture tip-overs and collapsing equipment are recalled because of what happens when weight moves, so an anchoring kit is a common remedy. Each notice says whether the fix is a free repair kit, a refund, or stopping use entirely.
589 stored notices, reported between Aug 15, 2012 and Oct 29, 2026. Newest first.
Reported Oct 1, 2014
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pdg Product Design Group Inc.
FDA (openFDA device enforcement)
Reported May 14, 2014
RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/ 2 motors); 763 (3 motors); 763 A ( 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-Mizer, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2014
The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArjoHuntleigh Inc.
FDA (openFDA device enforcement)
Reported Oct 23, 2013
GE Healthcare, Aisys, Amingo, Avance, and Avance CS2. Intended for volume or pressure control ventilation.
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral body replacement or intervertebral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kreg Medical Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Molift Smart 150
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moller Vital
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 16, 2013
FlowGate Balloon Guide Catheter; Manufactured by Concentric Medical, Mountain View, CA.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Concentric Medical Inc.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR 2107-0120 20mm Standard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Titan Spine, LLC
FDA (openFDA device enforcement)
Reported Nov 14, 2012
AC Powered adjustable hospital bed, Prime Bed TL500, Distributed by: Primus Medical LLC, 8401 Southern Blvd, Boardman,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Primus Medical LLC
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral body replacement system intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lucero Medical LLC
FDA (openFDA device enforcement)
Reported Aug 15, 2012
LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
1 more product in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.