State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Battery-Biz is recalling Cyntur CTJSLI Lithium Ion Jumpstarters because a faulty cable design may cause overheating and fire. Owners should contact customer service for a free replacement cable.
Jayco is recalling 10 model year 2016 White Hawk travel trailers because they were built with axles rated for 3000 lbs instead of the required 3500 lbs, which may affect handling.
Winnebago is recalling 2016 Instinct trailers because an incorrect character may be stamped in the VIN. Dealers will replace the VIN plate at no cost.
Arrow International is recalling Percutaneous Insertion Trays because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling RediGuard IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.
Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, posing a risk of bleeding.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling two syringes of Hydromorphone HCL 1 mg/ml because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Stryker is recalling Position Pro Mattresses because the power cord may melt, posing risks of electric shock and fire.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Baclofen syringes due to a lack of assurance of sterility. The affected products were distributed nationwide.
Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, creating a risk of bleeding.
Verathon is recalling GlideScope Titanium single-use video laryngoscope blades because the video image may flicker or distort during use.
Hartley Medical Center Pharmacy is recalling Baclofen 5000 mcg/ml syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone, baclofen, and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Winnebago is recalling certain 2015-2016 Adventurer and Itasca Suncruiser vehicles because hitch bolts were not properly torqued, which could cause the hitch to detach and increase crash risk.