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.
Munchkin is recalling Latch lightweight pacifiers and clips because the clip cover can detach, posing a choking hazard to young children.
Marathon Ventures Inc. is recalling macadamia nuts under seven brands because FDA testing found Salmonella in a retail package.
Roland Foods is recalling Fire Roasted Red Pepper Strips due to the possible presence of glass fragments in specific lots.
Kaufman is recalling 2015-2016 Flatbed Equipment and Wedge Car Hauler trailers because axle hanger lock nuts may loosen, potentially causing the axle to detach and increasing crash risk.
Health Matters America is recalling Organic Traditions Sprouted Chia & Flax Seed Powder due to potential Salmonella contamination.
Newmar is recalling 2015-2016 Ventana and Ventana LE vehicles because front sway bar brackets may not fit properly, risking bolt failure and loss of vehicle control.
Health Matters America is recalling Organic Traditions Sprouted Flax Seed Powder due to potential Salmonella contamination. Consumers should stop using the product.
Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.
Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.
NOW Foods is recalling 57 bottles of Elderberry 500 mg capsules because they contain undeclared soy lecithin, a common allergen.
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.
Becton Dickinson is recalling Trypticase Soy Agar and MacConkey II Agar plates contaminated with Listeria monocytogenes. The non-sterile media are used for growing and detecting bacteria.
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers because they malfunction when specific alarms appear on the system.
Elekta is recalling 217 Radionuclide Radiation Therapy Systems because frame adapter latches can lock without proper pin insertion, potentially compromising treatment accuracy.
Auto Truck is recalling 2013-2016 IMT Dominator Series III vehicles because a valve bank cover may crack and fall off, creating a road hazard.
Siemens is recalling 37 SOMATOM Force CT systems because a software error in the Neonate Head protocol may cause image artifacts, potentially leading to misdiagnosis.
NOW Foods is recalling Gingko Biloba 60mg capsules because they contain undeclared soy lecithin. Consumers should stop using the product and return it to the place of purchase.
NOW Foods is recalling 3 bottles of cranberry extract capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.
Volvo is recalling 2016 XC90 vehicles because the sunroof switch may be unintentionally pressed, causing the panel to close and increasing the risk of occupant injury.
NOW Foods is recalling Andrographis extract 400 mg capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.
Roche Molecular Systems is recalling 6,939 IT3800 hand-held barcode scanners because they mis-identified sample barcodes when used with the COBAS AmpliPrep instrument.
Philips and Neusoft are recalling 37 NeuViz 16 CT scanners due to a software defect that may allow previous patient images to be pasted into the current patient's record.
Shimadzu Medical Systems is recalling 185 X-Ray Diagnostic Tables (Model YSF-300) due to reports of unintentional movement to reverse tilting.
Intuitive Surgical is recalling 43 EndoWrist Stapler instruments for the da Vinci Xi system due to a risk of unexpected jaw motion during use.
NOW Foods is recalling Goldenseal Root 500 mg capsules because they contain undeclared soy lecithin, a common allergen.