State
73,576 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Maquet is recalling 667 PowerLED 300 Concealed Lighting Systems because the spring arm may detach and fall, posing a potential injury risk.
Abiomed is recalling 3,322 Automated Impella Controllers worldwide due to firmware and software defects that affect pressure signal accuracy and system reliability.
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Midmark Corporation is recalling 20 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Medline is recalling 234 neurological surgery kits nationwide due to potential endotoxin variability that may cause adverse health reactions.
Midmark Corporation is recalling 33 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
New York Embroidery Studio is recalling 5,400 Trinity Non-Surgical Isolation Gowns because they do not consistently meet minimum liquid-barrier performance requirements.
Cardinal Health is recalling 17,503 Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Olympus is recalling 2,142 BiCOAG Hemostasis Probes because a manufacturing error may cause the ceramic tip to detach.
Greenpower is recalling 94 EV Star buses because a software error may allow the vehicle to move while the wheelchair lift is deployed.
Midmark Corporation is recalling 153 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
SeaSpine Orthopedics is recalling 270 units of the Mariner Deformity Extended Polyaxial Head because the proximal thread depth is out of design specification.
Intervascular is recalling Cardioroot Woven Collagen Coated Vascular Grafts because the product failed to meet acceptance criteria for Integral Water Permeability.
Medline is recalling 486 craniotomy convenience kits due to potential endotoxin variability that may cause adverse health reactions.
Midmark Corporation is recalling IQvitals Zone devices because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Medline is recalling 695 convenience kits containing neurological sponges due to potential endotoxin variability that may cause adverse health reactions.
Amneal Pharmaceuticals is recalling 5,694 Exenatide Injection pens because the delivery system may be defective, potentially leaving the pen empty of medication.
Medline Industries is recalling 4,013 neurological surgery kits due to potential endotoxin variability that may cause adverse health reactions.
Cardinal Health 200, LLC is recalling Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Starcraft RV is recalling 2022-2024 Super Lite Maxx travel trailers because fasteners may fail, causing the fresh water tank to detach and create a road hazard.
Philips is recalling 387 Achieva 1.5T MRI systems worldwide because a software issue may terminate examinations if manual scan adjustments exceed system memory.
Ventec Life Systems is recalling 25 HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Baxter Healthcare is recalling six PRO+ 40-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label text.
Criticare Technologies is recalling 1,007 nGenuity Patient Monitors because a setup error renders the CO2 monitoring function inoperable, potentially delaying procedures.
Baxter Healthcare is recalling two VOLARA systems because contamination in test equipment may have affected flow rate accuracy. Affected devices were returned and confirmed to meet specifications.