State
72,913 recalls have nationwide distribution and so reach Arkansas. 5,513 additional recalls listed Arkansas specifically in their distribution scope.
Of the 5,513 recalls naming Arkansas we have scored against our rubric, 1,018 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,210 (22%) are Severe.
Which agencies issued them
These figures cover only the 5,513 recalls whose distribution notice names Arkansas specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.
Gudook Adult Bike Helmets (model KY-055, batch 202503, March 2025 manufacture) violate mandatory safety standards and fail to protect users in a crash, posing a serious risk of head injury or death. About 520 units sold on Amazon from May 2025 through February 2026.
Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.
Automated Impella Controllers sold outside the US are being recalled over alarm failures, power-path faults, electrical-short risks, inaccurate motor-current sensing and purge cassette misalignment.
Automated Impella Controllers that have not been through Abiomed's servicing process are pending four hardware updates addressing motor control, startup and pump stop risks.
Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.
Aston Martin is recalling 2024 Valkyrie vehicles with track suspension because a deforming brake seal can cause overheating and fire risk.
Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.
Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.
Medline anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 1,100 kits are affected.
Medline EYE TRAY-LF kits are being recalled because they contain Cardinal Health syringes packaged as 1 mL tuberculin syringes but which are actually U-100 insulin syringes.
HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.
Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
Jayco is recalling 2026 Melbourne Prestige and Entegra Qwest recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
Jayco is recalling 2026 Entegra and Jayco recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.
Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.
Medtronic 2x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64002, are being recalled because a limited number are labeled with incorrect use-by dates.
Medtronic 1x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64001, are being recalled because a limited number are labeled with incorrect use-by dates. 275 units are affected.
Pred Mild prednisolone acetate ophthalmic suspension 0.12% is being recalled after failing stability specifications. 2,736 bottles are affected.
Nicotine Transdermal System Patches, 14 mg, distributed by Rugby Laboratories are being recalled after elevated oxidative-related impurities exceeded shelf-life specifications.
Braun is recalling 2026 Ram ProMaster vehicles with specific wheelchair seat belts that may have incompatible connectors and fail to restrain occupants.