State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 19 ArComXL Polyethylene Bearings because packaging labels did not match the physical product inside, posing a risk of surgical delay.
Town and Country Compounding is recalling 101 vials of HCG because potency testing showed 74%, below the required 80-125% range.
Sandoz Inc. is recalling specific lots of Donepezil Hydrochloride 10 mg tablets because they failed potency tests. The medication may not contain the full prescribed dose.
Medacta USA Inc. is recalling 82 M.U.S.T. Rods due to damaged packaging and lack of sterility assurance. The recall covers units distributed in the US and several international countries.
Endologix is updating the Instructions for Use and implementing modifications to the AFX Endovascular AAA System.
Endologix is recalling the AFX2 Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.
L. Perrigo Company is recalling 162,534 tubes of Clindamycin Phosphate and Benzoyl Peroxide Gel because a small number of tubes may contain mold on the cap.
Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.
Endologix updated the Instructions for Use and modified the AFX Endovascular AAA System. The correction applies to procedures conducted after July 2015.
Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.
DICOM GRID Inc. is recalling Ambra PACS software version V3.16.13.0 because a defect causes diagnostic images to appear washed out, potentially affecting image analysis.
Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.
Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.
Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.
Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.
Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.
HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.
Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.
Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.
Pulse Performance is recalling about 8,900 children's electric scooters sold at Target because a wheel component can break, posing a fall hazard to riders.
Autocar is recalling 38 Xpeditor trucks from 2013-2016 because over-braking can cause S-cam tube bolts to loosen, leading to unexpected brake engagement and increased crash risk.
IH Parts America Inc. is recalling specific steering tie rod adjusters for International Scout vehicles because they may fracture, affecting steering capability and increasing crash risk.
Autocar is recalling 2016-2017 Xspotter vehicles because they lack a dimmer switch for dash illumination, which may increase crash risk.
BMW is recalling specific 2000-2003 3, 5, and X5 series vehicles because replacement driver-side air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.