State
73,106 recalls have nationwide distribution and so reach Arizona. 8,386 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,386 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 1,720 (21%) are Severe.
Which agencies issued them
These figures cover only the 8,386 recalls whose distribution notice names Arizona specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Autocar is recalling 2020-2024 Legend vehicles because hazard warning lights may not function when the ignition is off, increasing crash risk.
About 19,264 Intimidator and Mahindra UTVs are recalled because the universal joint can fail and sever the brake line, posing a crash hazard. No injuries have been reported. Owners should immediately stop using the vehicles and contact a dealer for free repair.
About 356 Touchat Large Fuzzy Area Rugs sold on Amazon.com violate federal flammability regulations and pose a fire hazard. Consumers should stop using them immediately and contact Touchat for a refund.
Fischer Sports is recalling RC4 Junior Ski Boots because the cuff can rotate and cause the lock mechanism to fail, creating a fall hazard. Consumers should stop using them immediately and contact Fischer for a refund, replacement, or repair.
Innovative Bedding Solutions and SBL are recalling about 1,250 GhostBed Natural mattresses because they violate federal flammability standards and pose a fire hazard. Consumers should stop using the mattresses and contact GhostBed for a free compliance cover.
Delta Cycle and Dimension Stem Raisers can shift during use, causing handlebars to move unexpectedly and creating a fall hazard. About 500,000 units sold nationwide from January 1998 through January 2024.
SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.
SleepNet is recalling the Phantom 2 Nasal Vented Mask to update contraindications and warning information related to magnets in the device. The recall affects 2,417 units distributed worldwide.
SleepNet Corporation is recalling 23,042 Mojo Full Face CPAP masks worldwide because the masks contain magnets that require updated contraindications and warning language.
SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.
SleepNet Corporation is recalling Mojo 2 Full Face Non Vented Masks due to magnets in the device and updated contraindications and warnings. The recall affects 2,107 units distributed worldwide.
SleepNet Corporation is recalling Mojo 2 Full Face CPAP masks (1,268 units worldwide) to update contraindications and warning language due to magnets in the masks. The FDA classified this as a Class I recall.
Hi-Tech E.V.S. is recalling 2020-2023 Spartan Gladiator and Metrostar fire trucks because a firmware defect in specific nodes may cause electrical circuits to overheat and increase the risk of fire.
SleepNet Corporation is recalling the iQ 2 Nasal Vented Mask due to magnets requiring updated contraindication and warning language. Approximately 2,477 units distributed worldwide are affected.
Technicality Inc. is recalling Trumpet Needle Guides (Cat# TMS-200) because the ring can detach when excessive pressure is applied. Approximately 20,000 units distributed nationwide in Illinois are affected.
Medline Industries is recalling Centurion surgical scissors due to potentially weak seals that may compromise sterility. Users cannot reliably detect the defect, creating risk if compromised instruments are used in surgery.
Medline Industries is recalling 1700 Centurion Sterile Trach Brush devices due to a potential weak seal that may breach product sterility if the seal fails. The defect may not be obvious to users.
Exactech humeral liners used in shoulder replacement are recalled because the vacuum packaging lacks a required oxygen barrier layer (EVOH), violating established packaging specifications.
Coloplast Manufacturing is recalling 710 ureteral dilators due to a possible breach in sterile packaging detected during facility testing. The devices are distributed across multiple US states.
Covidien is recalling approximately 11,796 Auto Suture Blunt Tip Trocar units due to potential seal disengagement when mesh products are used incorrectly with the device. The issue could occur during surgical procedures.
Medline is recalling Centurion manual surgical kits with potentially weak seals that may result in a breach of sterility if the seal fails. The weak seal may not be detectable by all users.
Medline Industries is recalling Centurion manual surgical kits due to weak seals that may compromise sterility. Approximately 7,950 units were distributed nationwide and internationally.
Covidien Auto Suture Blunt Tip Trocar devices are recalled due to potential seal disengagement when using mesh products incorrectly with the device. This malfunction risk affects surgical procedures.
Exactech is recalling 245 units of shoulder implants due to nonconforming packaging that lacks a required oxygen barrier layer. The devices were distributed nationwide and internationally.
Covidien is recalling certain Signia surgical stapler reloads due to unsecured components that can cause uncontrolled articulation during use, potentially disrupting the staple line. The recall affects 3,023 units distributed worldwide.