State
73,576 recalls have nationwide distribution and so reach Arizona. 8,391 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,391 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 2,047 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline Industries is recalling Basic and Medlite Homecare Beds due to a potential fire hazard involving the hand control pendant and wiring.
Draeger is recalling VentStar Resus Neo neonatal breathing circuits due to potential hose cracks that could cause leakage or disconnection.
BMW is recalling 2021-2024 R 18 motorcycles with optional reverse gear because a deteriorating seal may allow moisture to enter the control unit, causing overheating and increasing the risk of a fire.
Penumbra Inc. is recalling 43 RED 62 Reperfusion Catheters due to manufacturing issues that may cause the catheters to fracture.
Par Health USA is voluntarily recalling 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. The FDA classifies this as a Class II recall.
American Contract Systems Inc. is recalling 1,804 medical kits containing BD CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Heraeus Medical GmbH is recalling PALACOS R+G pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall affects 59,660 units distributed worldwide.
American Contract Systems Inc. is recalling 1,804 medical convenience kits containing potentially contaminated perineal care wipes. The contamination may cause skin irritation or increase infection risk.
Percussionaire Corporation is recalling Travel Air and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Cardinal Health 200, LLC is recalling 344 Presource Packs containing Stryker tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Heraeus Medical is recalling PALACOS R pro 40 and 80 bone cement because of a potential for monomer liquid leakage. The recall affects 33,727 units distributed worldwide.
American Nitrile Operations LLC is recalling 17,481,000 Opportunity Pro nitrile gloves nationwide due to defects like tears and debris that may expose users to pathogens or chemicals.
Cardinal Health is recalling 3,677 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Heraeus Medical is recalling PALACOS MV pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall covers all lot numbers distributed worldwide.
Shanghai United Imaging Healthcare is recalling four uCT 530 CT systems due to a software defect that may hide patient images, potentially requiring rescans.
Bard Peripheral Vascular Inc is recalling 99 EnCor EnCompass Breast Biopsy and Tissue Removal Systems due to software errors that may interrupt procedures.
Merit Medical Systems is recalling Embosphere microspheres because packaging holes may compromise sterility, posing an infection risk.
Alere San Diego is recalling hCG rapid test cassettes because they may detect low hormone levels, leading to false positive pregnancy results.
Percussionaire Corporation is recalling Impulsator and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Tandem Diabetes Care is recalling a beta version of its t:slim iOS app because it fails to pair with Abbott FreeStyle Libre 3 Plus sensors, forcing users into manual mode.
Siemens Healthcare Diagnostics is recalling Atellica CH Revised C-Reactive Protein reagent due to the potential for falsely elevated test results.
American Nitrile Operations is recalling Performance Pro blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
Alere San Diego is recalling multiple hCG urine pregnancy test models because they may detect low hCG levels, resulting in false positive results.
NOXBOX LTD is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems due to a manufacturing issue that may cause irregular oxygen readings.
Percussionaire Corporation is recalling 98,434 In-Line Valves to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.