State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Comfort Gel Cherry Flavor because the product failed the Antimicrobial Effectiveness Test.
Attix Pharmaceuticals is recalling Homatropine Methylbromide active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.
Biomet Spine is recalling 874 Torque Limiting Handles used in spinal fixation due to supplier component updates.
Specialty Appliance Works is recalling Universal Nuts for MiniScope Mechanical Sets because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Specialty Appliance Works is recalling Herbst Universal Nuts because they were manufactured with 416 SS instead of the specified 303 SS.
Specialty Appliance Works is recalling TS Herbst Nuts because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.
Specialty Appliance Works is recalling TS ROC Crown Components because the Universal Nut was made with 416 SS instead of the specified 303 SS.
Specialty Appliance Works is recalling Universal Nuts used in Herbst orthodontic appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Attix Pharmaceuticals is recalling Piperacillin Sodium active pharmaceutical ingredient because it was repackaged without data supporting the printed expiry date.
Attix Pharmaceuticals is recalling Amoxicillin Trihydrate active pharmaceutical ingredient because stability data does not support the printed expiry dates.
Specialty Appliance Works is recalling Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.
Biomet Spine is recalling 148 Lineum HF Torque Handle Limit units because the supplier withdrew the product for component updates or reconfiguration.
Attix Pharmaceuticals is recalling Procaine Penicillin G active pharmaceutical ingredient because stability data does not support the printed expiry dates on repackaged lots.
Walong Marketing is recalling Wu Fu Yuan Sago Taro because it contains unapproved FD&C Red #2.
Specialty Appliance Works is recalling Universal Nuts for orthodontic Herbst Appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Attix Pharmaceuticals is recalling Ticarcillin Sodium/Potassium Clavulanate API because stability data does not support the printed expiry dates for lots distributed between 2012 and 2015.
Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Antacid Liquid because the product failed the Antimicrobial Effectiveness Test.
SpineFrontier is recalling the MISquito Pedicle Screw System Surgical Technique document because it does not adequately convey the intended use of the Rod Caliper.
Tarmac Products, Inc. is recalling 41,743 bottles of Well at Walgreens Maximum Strength Comfort Gel because the product failed the Antimicrobial Effectiveness Test.
Nomax Inc. is recalling GLOSTRIPS ophthalmic strips because packaging degradation may affect the uniformity of the rose bengal dosage.
Nomax Inc. is recalling GLOSTRIPS and FUL-GLO ophthalmic strips because packaging degradation may affect dosage uniformity. No illnesses have been reported.
Nomax Inc is recalling Fluorescein Sodium Ophthalmic Strips because packaging degradation may affect dosage uniformity. The recall covers 62,691 cartons distributed in the US and internationally.
Reckitt Benckiser is recalling Mucinex DM extended-release tablets due to a defective seal on the top of the pouch.
Whistler is recalling about 10,400 Jump&Go portable jumpstart power supplies because the lithium battery can overheat, melt, and catch fire.
Mastercraft is recalling 1,740 model year 2015 boat trailers because the tongue bolt may fail, allowing the trailer to disconnect from the tow vehicle and increasing crash risk.