State
73,100 recalls have nationwide distribution and so reach Arizona. 8,385 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,385 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,719 (21%) are Severe.
Which agencies issued them
These figures cover only the 8,385 recalls whose distribution notice names Arizona specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Abbott is recalling 1198 Infinity 7 Implantable Pulse Generators due to potentially incorrect service life indicators and end-of-service dates in product labeling, which could result in loss of therapy.
A software issue in certain Siemens Sensis Vibe diagnostic systems may cause the application to crash when documentation features are used during clinical reporting events.
Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.
Medtronic recalled A610 Clinician Programmer software and pocket adaptors (Models 64001, 64002) due to MRI safety restrictions. Patients with these implants are limited to head-only MRI procedures.
Abbott Infinity 5 implantable pulse generators have inaccurate end-of-service dates in labeling, which may result in loss of therapy. Approximately 5,900 units are affected and distributed worldwide.
Medtronic is recalling 636 units of TourniKwik Tourniquet Sets due to incorrect components placed in four manufactured lots. Distribution includes the US states of Minnesota, Massachusetts, Utah, California, Florida, Japan, and Slovenia.
Olympus is recalling 86 ESG-410 Electrosurgical Generators because they may fail to power on during use, potentially delaying treatment or prolonging surgery.
Sweet Preserved Dried Plums from Farmer's Grange contain undeclared cyclamate sweetener. The product was distributed in select U.S. states and should not be consumed.
Siemens Sensis Vibe diagnostic systems may crash when documentation functionality is used during certain reporting events. Seven units were distributed to facilities nationwide.
FDA Class III recall of Nature's Script CBD Cryotherapy Pain Relief Roll-on (200mg, 1 oz bottles) due to subpotent menthol content less than the labeled 4%. The product did not contain the claimed amount of active ingredient.
Hemp Bombs CBD Pain Freeze is being recalled because the menthol content is weaker than the labeled 4% claim. The recall affects 2,082 bottles distributed nationwide.
Avanos Medical is recalling MIC-KEY Gastric-Jejunal Feeding Tube Kits because the Instructions for Use were missing required risk information about potential complications. No illnesses have been reported.
Hemp Bombs CBD Pain Freeze is being recalled because the menthol potency is less than the labeled 4%. Consumers should stop using the affected product and return it to the retailer.
Randox Laboratories is recalling 115 kits of RX Series CYSC Cystatin C Reagent because it was marketed without required FDA 510(k) clearance. Healthcare facilities should discontinue use and contact the manufacturer.
Global Widget LLC is recalling Hemp Bombs CBD Pain Freeze (4% menthol) because the menthol concentration is below the labeled claim. Approximately 11,130 bottles were distributed nationwide.
Washington Homeopathic Products is recalling 11 Complete 30C/200C Homeopathic Kits nationwide due to a labeling error. Some bottles labeled as Ferrum Metallicum 200C actually contain Ferrum Phosphoricum 200C.
Boar's Head is recalling 7 million pounds of ready-to-eat meat and poultry products due to possible Listeria contamination linked to a multistate outbreak.
Mevotech is recalling specific aftermarket front lower control arms because a design flaw may cause the ball joint to separate, increasing crash risk.
Mack is recalling certain 2024-2025 Anthem, Granite and Pinnacle vehicles with RollTek driver's seats because the seat pedestal and seat belt attachment may have been improperly tightened.
Tiffin is recalling certain 2022-2025 Phaeton, Allegro Bus and Zephyr motorhomes because the PowerGlide chassis controller may have insufficient circuit protection, which can blow a fuse and shut down the engine.
Boar's Head Provisions is recalling liverwurst and other deli meats nationwide due to possible Listeria monocytogenes contamination linked to a multistate outbreak.
Meritor is recalling replacement tie rods with specific USK ball studs that may break due to incorrect heat treatment, risking loss of steering control.
Nova Bus is recalling certain 2019-2023 LFS and LFS Artic buses because the glazing used on the glass windows may reduce the driver's visibility, failing FMVSS 205.
Forest River is recalling 2025 Cherokee CKT20-0G travel trailers because an incorrect screw in the microwave compartment can cause electrical arcing and fire.
BMW is recalling certain 2024 R 1300 GS motorcycles because the starter motor relay housing may have been manufactured incorrectly, resulting in a damaged relay that can overheat.