State
72,940 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.
Which agencies issued them
These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Somerset Therapeutics is recalling 52,340 vials of Cisatracurium Besylate Injection, 10 mg/5 mL, after out of specification assay results during long term stability testing.
Somerset Therapeutics is recalling 28,660 vials of Cisatracurium Besylate Injection, 200mg/20mL, after out of specification assay results during long term stability testing.
Novocol Pharmaceutical of Canada is recalling 18,789 cartons of 2% Xylocaine Dental with Epinephrine over a defective container with cracked or broken cartridges.
DSAART is recalling 369 AART Silicone Carving Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Novocol Pharmaceutical of Canada is recalling 1,636 cartons of OraVerse (Phentolamine Mesylate) Injection over a defective container with cracked or broken cartridges.
Smith & Nephew is recalling 168 BIOSURE HA Screws, 6mm x 20mm, due to a labeling error on the affected lot.
DSAART is recalling 118 AART Gluteal Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Myofunctional Research Company USA is recalling 436 Myosa for Kids devices because the firm mistakenly distributed the product within the US without FDA premarket clearance or approval.
DSAART is recalling 41 AART Pectoral Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
DSAART is recalling 2 AART Malar Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Novocol Pharmaceutical of Canada is recalling 5,520 cartons of Mepivacaine HCl 3% injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling 5,825 units of 3% Polocaine Dental mepivacaine injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling Mepivacaine HCl 3% injection distributed by Benco Dental over a defective container with cracked or broken cartridges.
Datascope is recalling 47 Cardiosave Rescue units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Datascope is recalling 11,470 Cardiosave Hybrid units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.
Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.
KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.
Honda is recalling certain 2024-2025 CBR650R motorcycles because engine vibration may damage the turn signal switch wire harness, causing a short circuit and a blown fuse.
Tiffin is recalling certain 2025-2026 Open Trail motorhomes fitted with an optional diesel or propane generator because the wiring harness may contain incorrectly sized wires.
Spartan Fire is recalling certain emergency vehicles because a ladder handle may detach, allowing ground ladders to fall off and creating a road hazard.
Volvo is recalling certain 2021-2025 vehicles across the XC40, XC60, XC90, S60, S90, V60 and V90 ranges because the rearview camera image may not display when the vehicle is in reverse.
Nissan is recalling 2026 Rogue vehicles with an incorrect-size spare tire that does not match the tire placard information. This may lead to improper tire inflation and increased crash risk.
TICO is recalling 2018-2026 Pro Spotter Tandem tractors because a track rod mounting bracket may crack and break, potentially causing loss of steering control.
Couture Co is recalling four models of Volt e-bike carriers because the latch mechanism may wear excessively and disengage while driving.