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.
RH Baby & Child is recalling about 480 Jeune French Contemporary Upholstered Panel Cribs because cylindrical metal inserts in the wooden frame can become loose and detach, posing a choking hazard to infants.
Brompton T-Line Foldable Bicycles are recalled because loose steerer clamp bolts can cause misalignment between the handlebar and front wheel, risking loss of steering control and falls. About 1,080 units are affected.
ECHO Inc. is recalling about 3,900 gas-powered backpack blowers due to a fuel supply line that can leak gas, creating a fire hazard. No injuries have been reported.
The left rear seat back in certain 2023 Dodge Charger vehicles may not lock in the upright position. This creates a risk of injury in a crash.
General Motors is recalling 2024 Chevrolet Malibu vehicles that may have an incorrect owner's manual. The wrong manual could contain inaccurate vehicle safety information.
Jayco is recalling 2025 Entegra Cornerstone motorhomes because inadequate fuse protection on chassis batteries increases the risk of a fire.
Medtronic Xomed is recalling NIM Vital Nerve Monitoring systems because they may fail to detect nerve damage or dysfunction. Approximately 7,804 units were distributed worldwide.
Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.
B Braun is recalling Perfusor Space syringe pumps because manufacturing changes to Cardinal Health Monoject syringes may cause incompatibility, resulting in dosing errors or delayed treatment.
Olympus is recalling 86 ESG-410 Electrosurgical Generators because they may fail to power on during use, potentially delaying treatment or prolonging surgery.
B Braun Medical's Perfusor Space Syringe Pump may not properly recognize Cardinal Health Monoject syringes due to manufacturing changes, risking medication overdose, underdose, or therapy delays.
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.
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.
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.
Universal Bakery Organic Sunrise Energy Bars labeled as gluten-free but found to contain gluten above FDA limits. The product poses a risk to consumers with celiac disease or gluten sensitivity.
Best Express Foods is recalling Universal Bakery Organic Aussie Bites due to undeclared gluten. Products labeled as gluten-free were found to contain gluten above regulatory limits.
Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.
Zydus Pharmaceuticals (USA) Inc. is recalling Venlafaxine Hydrochloride Extended-Release Capsules USP 37.5mg due to failed dissolution specifications in lots M213175 and M213176. The recall affects 13,128 and 252 bottles distributed nationwide.
The Abbott Infinity 7 implantable pulse generator's replacement indicator and end-of-service date may be shorter than the product labeling states, potentially leading to loss of therapy for patients.
B Braun is recalling Perfusor Space infusion pump kits because Cardinal Health Monoject syringes have manufacturing changes that make them incompatible, potentially causing overdose, underdose, or delayed therapy.
B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.
Radiometer Medical ABL800 FLEX blood gas analyzers (models 393-800, 393-801) may report inaccurate pH results due to bacterial growth in calibration solution bottles. Approximately 27,127 units distributed worldwide are affected.
Canadian Art Prints is recalling Indigenous Collection Signature Plates sets because the glazed ceramic plates may exceed FDA guidance levels for leachable lead. Consumers should stop using these plates immediately.
B Braun is recalling Perfusor Space infusion pumps due to syringe compatibility issues with Cardinal Health Monoject syringes. The incompatibility may cause overdose, underdose, therapy delays, and alarm failures.
Beckman Coulter is recalling 143 Dxl 9000 Immunoassay Analyzers due to nonconforming USB cables with brass instead of gold contacts. Brass may corrode, potentially disabling internal communication and delaying patient test results.