State
73,584 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toyworld168 is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Tongyang Cycling is recalling Basecamp bicycle helmets because they violate mandatory safety standards, posing a risk of serious head injury or death.
Esjay is recalling toddler busy board toys because red knobs can detach, posing a choking hazard to children under three.
Char-Broil is recalling about 10,605 Bistro Pro Electric Grills because a grounding wire can disconnect, posing an electric shock hazard. No injuries have been reported.
SHEIN is recalling Pull & Chew Montessori Teething Toys because the silicone strings violate safety standards and pose a choking risk. No injuries have been reported.
Melissa & Doug is recalling about 84,000 Lights & Sounds Fire Truck Activity Board toys sold at Target and Amazon because a fire hose port can detach, posing a choking risk.
B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide and fibers.
American Regent, Inc. is recalling 31,935 vials of Epinephrine Injection due to the presence of particulate matter and broken vials.
Rewaco is recalling 106 three-wheeled motorcycles because a rear shock absorber connection may loosen, potentially causing a loss of vehicle control.
Nipro Renal Solutions is recalling MedicaLyte Liquid Bicarbonate Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Nipro Renal Solutions is recalling Citric Complete Liquid Citric Acid Concentrate due to high endotoxin levels. The product was distributed in the US and internationally.
Baxter Healthcare is recalling 606 bags of Dextrose Injection, USP, 70% due to the presence of stainless steel particles in the solution.
Given Imaging is recalling Bravo CF capsule delivery devices because they may fail to attach to the esophagus or detach from the device, posing risks of aspiration and perforation.
Nipro Renal Solutions is recalling Citric Complete Dry Citric Acid Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Rivian is recalling 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles because a notification may obstruct the rearview camera image, increasing crash risk.
Lutronic Corporation is recalling 1,065 DermaV Laser Systems because using higher fluences at 1064nm with current cryogen parameters may cause sparks or loud noise, potentially resulting in patient burns.
C.R. Bard is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
AVID Medical is recalling 98 Halyard IV Start Kits because wrinkles in the paper lidding may breach the seal, compromising sterility assurance.
Atrium Medical is recalling specific lots of Getinge PVC Thoracic Catheters because one lot failed bacterial endotoxin testing.
C.R. Bard is recalling SureStep Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
C.R. Bard is recalling 12,463 Foley and intermittent catheter trays because complaints indicated contamination on the surface of the included Pericare wipes.
C.R. Bard Inc. is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
Windstone Medical Packaging is recalling 3,260 AMS Convenience Kits because the included sodium chloride bags may contain detached blue break-off parts.
HeartSine Technologies is recalling SAM 350P, 360P, and 450P defibrillators due to a damaged membrane tail that causes intermittent faults.
Atrium Medical Corporation is recalling specific lots of Getinge PVC Thoracic Catheters because bacterial endotoxin testing results were out of specification.