State
73,827 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Amax is recalling Bostitch electric pencil sharpeners because internal components can energize the unit, posing a shock hazard. One consumer reported receiving a shock.
Micro Bird is recalling 2006-2014 transit buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Coach and Equipment is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts. The lifts may have pivot holes that allow bearings to move, risking platform failure.
Forest River is recalling specific 2012-2016 recreational vehicles because a water heater valve may cause overheating, potentially leading to steam release and scalding injuries.
Gillig is recalling Ricon Model S5510 wheelchair lifts because oversized pivot holes may allow bearings to shift, potentially causing the platform to fall and injure the operator.
Kingmor is recalling 271 IC CE school buses equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure operators.
The One Minute Miracle Inc. is recalling Miracle Rock 48 capsules because they contain undeclared thiosildenafil, an unapproved drug analogue.
The One Minute Miracle Inc. is recalling Miracle Diet 30 capsules because they contain undeclared phenolphthalein, an unapproved drug ingredient.
The Compounder is recalling specific lots of Biest TD 91/9 transdermal cream because the active ingredient was contaminated with penicillin.
The Compounder is recalling Biest CP 76/24 DHEA capsules because an active ingredient was contaminated with penicillin. The recall is nationwide.
The Compounder is recalling Biest TD 67/33 transdermal cream because the active ingredient was contaminated with penicillin. The recall covers 10 syringes per lot distributed nationwide.
The Compounder is recalling Biest TD 80/20 transdermal cream because it was made with an active ingredient contaminated with penicillin.
Boston Scientific is recalling RotaWire Elite Guidewires and wireClip Torquer devices due to complaints of wire fracture. The devices are used with the Rotablator Rotational Atherectomy System.
The Compounder is recalling specific lots of a compounded transdermal hormone cream because the active ingredient was contaminated with penicillin.
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin.
The Compounder is recalling Biest TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
The Compounder is recalling Biest TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
The Compounder is recalling Biest TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin. Patients should stop using the product and consult their healthcare provider.
The Compounder is recalling BIEST TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin by a supplier.
The Compounder is recalling Estradiol and Testosterone transdermal cream because the active ingredient was contaminated with penicillin.
The Compounder is recalling Biest TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin. This recall affects nationwide distribution.
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
The Compounder is recalling BIEST TD 50/50 transdermal cream because the active ingredient was contaminated with penicillin by a supplier.
The Compounder is recalling Estriol 4.0mg capsules because the active ingredient was contaminated with penicillin. Patients should stop using the product and consult a healthcare provider.