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.
Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.
Toyota is recalling 949 model year 2015 Prius C vehicles because the tire pressure monitoring system may fail to warn drivers of low tire pressure, increasing crash risk.
Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because the tips may split or separate, potentially causing loss of function or complications.
Anabolic Science Labs is recalling Slim X Lean Hour 12+ Hour Energy products due to undeclared synthetic hormone ingredients.
Cook Inc. is recalling Beacon Tip Royal Flush Plus High-Flow Catheters due to reports of tip splits or separation that may cause loss of function or complications.
Medtronic is recalling 1,415 Passive Biopsy Needle Kits because adhesive failure may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.
Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.
Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.
Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.
Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.
Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.
Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.
Pierce is recalling 2014-2015 Velocity and Quantum vehicles because LED headlamps may flicker in extreme cold, reducing visibility and increasing crash risk.
Flowers By Zoe is recalling girls' striped hoodies and tie-dye jackets because neck drawstrings pose a strangulation hazard to children.
Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.
Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.
Nissan is recalling 2012-2015 Versa and 2014-2015 Versa Note vehicles because a center console trim panel may catch the driver's shoe, delaying brake application and increasing crash risk.
Teva Pharmaceuticals is recalling specific lots of amphetamine tablets because they failed impurity specifications. The product contains an unknown impurity.
Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.
Chrysler is recalling 2014 Jeep Cherokee vehicles because using front wipers on dry glass may damage the body control module, potentially causing wiper failure and impaired vision.
Mondelez International is recalling Nabisco Fig Newtons because the outer carton fails to declare milk, a major allergen, while the inner packaging does.
Winnebago is recalling 2014-2015 Itasca and Winnebago motorhomes because deadbolt locks may become stuck, potentially trapping occupants inside the vehicle.
Philips is recalling 13,168 HeartStart XL+ defibrillators worldwide due to software and hardware issues that can affect device function.
Olympus Scientific Solutions Americas is recalling 1,047 Analytical X-ray Systems because scatter readings around the probe head were higher than published specifications for certain samples.
Ranbaxy Inc. is recalling 9,229 boxes of Absorica LD (isotretinoin) capsules because the capsule shells contain undeclared FD&C Yellow No. 5.