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.
Ossur Americas is recalling Rebound Cartilage knee braces and other medical devices due to a defect described in the source text.
Siemens is recalling 1,757 AXIOM Artis angiography systems because a possible leak in the cooling system could allow fluids to seep into the equipment cabinet.
Siemens is recalling 986 AXIOM Artis zee/zeego angiography systems because a cooling system leak could cause equipment failure.
Ossur Americas is recalling Rebound Air Walkers and other medical devices due to a defect described as 'the p'.
Ossur Americas is recalling various orthopedic braces and medical devices, including the Unloader Custom Lite, due to a defect described in the source text.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction hazard when using specific cardio licenses.
ProSupps USA LLC is recalling Dr. Jekyll Intense Pump Pre Workout because it may contain the non-dietary ingredient Picamilon.
Ossur Americas is recalling various orthopedic braces and medical devices, including knee braces and back supports, due to a defect described as 'the p'.
Siemens Medical Solutions is recalling 89 Cios Alpha mobile X-ray systems due to software issues. The units were distributed nationwide to 30 states.
Siemens is recalling four Cios Alpha mobile X-ray systems because a defective part could increase the risk of electrical shock for service personnel during maintenance.
Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.
Ossur Americas is recalling various medical devices, including Miami J collars and knee shields, due to a manufacturing defect.
Ossur Americas is recalling various medical devices, including knee braces and walkers, due to unspecified product issues.
Philips Medical Systems is recalling 4,180 foot switches used with Allura Xper systems because a bent pedal can cause loss of key image functionality.
Ventura Foods is recalling various brands of 35 lb. liquid fry shortening because plastic from the jugs may have entered the product.
Medtronic is recalling Reveal LINQ insertable cardiac monitors because an algorithm issue may trigger replacement alerts prematurely. The device battery and data collection capabilities remain functional.
Implant Direct Sybron is recalling GoDirect Implants because some consignees received the wrong tool to drive the implant to bone level.
Siemens is recalling 1,757 Artis zee/zeego angiographic X-ray systems because a possible leak in the cooling system could allow fluids to seep into the equipment cabinet.
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
Ventura Foods is recalling 35 lb. jugs of cooking oil because plastic fragments may be present due to a manufacturing defect in the jugs.
Siemens is recalling 3,090 E.CAM gamma camera systems to provide supplemental instructions and visual aids for proper collimator changes.
Biomet Spine is recalling specific Solitaire Ti Spacers because they are mislabeled as having a 12-degree lordotic angle when the actual angle is 6 degrees.
Siemens is recalling one Artis One angiography system because imported left atrium segmentation results may be incorrectly mirrored to a 3D mapping system.
Siemens is recalling 726 Symbia gamma camera systems worldwide to provide supplemental instructions clarifying the proper collimator change procedure.
Praxair Inc. is recalling 127 cylinders of compressed medical air because a customer reported an odor when turning on a cylinder.