State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling Stryker 15mm drills because an investigation found they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific 3.5mm orthopedic drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling 2.7mm AO surgical drills because they may have been manufactured from a material different from specifications.
Zimmer GmbH is recalling specific orthopedic drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling CBS 4.5 countersinks because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.
Zimmer GmbH is recalling 2.5x135mm AO Drills because they may be made from a different material than specified. The products were distributed to 41 US states.
Zimmer GmbH is recalling Drill Sys 2.7 units because they may have been manufactured from a material different from specifications.
Zimmer GmbH is recalling V-TEK IVP step drills because they may be made from a different material than specified.
Zimmer GmbH is recalling specific 2.7mm orthopedic drills because an investigation found they may be made from a different material than specified.
Aegean Apparel is recalling children's robes and pajama pants that fail to meet federal flammability standards, posing a risk of burn injuries.
Zimmer GmbH is recalling specific 19mm orthopedic drills because they may be made from the wrong material. The devices were distributed to 38 US states.
Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling 2.7x125mm AO drills because they may be made from the wrong material. The devices were distributed to 40 US states.
Zimmer GmbH is recalling Stryker 26mm drills because they may be made from the wrong material. The products were distributed to 39 US states.
Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.
ITI is recalling 2018-2019 HINO 268 and 338 vehicles because backup camera displays may revert to factory settings, causing reversed images and increasing crash risk.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling CBS 7.5 taps because they may be made from the wrong material. The products were distributed to 41 US states.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified. The products were distributed to 41 US states.
LGE Coachworks is recalling 2018-2019 Ford and Freightliner vans because back-up camera displays may revert to factory settings, reversing the image and increasing crash risk.
PL Custom is recalling 2017-2019 Type I and III ambulances because backup camera monitors may revert to factory settings, reversing the image and increasing crash risk.