The Recall Desk

State

Oklahoma product recalls

72,820 recalls have nationwide distribution and so reach Oklahoma. 5,785 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,785
Critical
1,031
Severe
1,237
Most recent
2026-09-02

Of the 5,785 recalls naming Oklahoma we have scored against our rubric, 1,031 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,237 (21%) are Severe.

These figures cover only the 5,785 recalls whose distribution notice names Oklahoma specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

326–350 of 78605

  • HighCPSC·26698·2026-08-13

    CuberShop Magnetic Speed Cubes Recalled Over Magnet Ingestion Hazard

    CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.

    Product
    CuberShop Magnetic Stickerless Speed Cubes, model YJ MGC 5×5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26691·2026-08-13

    Deli Jerry Fuel Containers Recalled Due to Burn Hazard and Child Poisoning Risk

    Deli Jerry fuel containers sold on Walmart.com are recalled because their caps are not child-resistant, posing burn and poisoning risks to children. No injuries have been reported; consumers should stop using them and contact Deli OfficeSupplies for a refund.

    Product
    Deli Jerry Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26696·2026-08-13

    Ritchey Recalls Carbon Bicycle Forks Due to Fall and Crash Hazard

    Ritchey Design is recalling about 775 carbon bicycle forks because the alloy insert in the crown hole can come loose, letting an accessory fall onto the front wheel and cause a crash. No injuries have been reported.

    Product
    Ritchey Carbon Fiber Bicycle Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26695·2026-08-13

    Qabefy Mattresses Recalled Due to Fire Hazard; Violate Flammability Standard

    Qabefy twin mattresses sold on Amazon are recalled because they violate the federal flammability standard, posing a fire hazard. Consumers should stop using them and contact Qabefy for a refund.

    Product
    Qabefy Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26699·2026-08-13

    SUGIFT Pressure Washers Recalled for Shock and Electrocution Hazards

    SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.

    Product
    SUGIFT Electric Pressure Washers, Model LTBBHG006
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V530000·2026-08-13

    GM Recalls 2024-2025 Silverado and Sierra 2500 Tires

    General Motors is recalling 2024-2025 Chevrolet Silverado 2500 and GMC Sierra 2500 trucks because incorrect tire pressure labels may cause underinflation and prevent low-pressure warnings.

    Product
    GMC — GMC, CHEVROLET SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V531000·2026-08-13

    Chrysler Recalls 2026-2027 Vehicles for Rearview Camera Display Failure

    Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.

    Product
    RAM — RAM, CHRYSLER, JEEP PROMASTER BEV, PACIFICA, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26689·2026-08-13

    TooyBing Wooden Bead Stacking Toys Recalled Due to Choking Hazard

    TooyBing is recalling its Wooden Bead Stacking Toys because the wooden beads pose a choking hazard to children under three years old.

    Product
    TooyBing Wooden Bead Stacking Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V529000·2026-08-13

    Chrysler Recalls 2026 Jeep Grand Cherokee Models for Wiper Software Issue

    Chrysler is recalling 81 2026 Jeep Grand Cherokee and Grand Cherokee L vehicles because a software issue may cause windshield wipers to fail, reducing visibility.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2797-2026·2026-08-12

    Halyard Convenience Kits Recalled Due to Particulates in Manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0743-2026·2026-08-12

    Cyclophosphamide Injection Recalled Due to Stainless Steel Particulate Matter

    Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.

    Product
    Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2796-2026·2026-08-12

    Halyard convenience kits recalled due to potential particulates in manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2891-2026·2026-08-12

    Philips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives

    Philips is recalling 5,012 Allura interventional fluoroscopic X-ray systems nationwide due to potential loss of imaging functionality, motorized movement, or data caused by unauthorized hard disk drives.

    Product
    Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2900-2026·2026-08-12

    GEM Premier 5000 PAK Lysing Solution Concentration Recall

    Specific lots of the GEM Premier 5000 PAK lysing bag solution have an active ingredient concentration that does not meet manufacturing specifications, which could delay recognition and management of Co-Oximetry and total bilirubin abnormalities.

    Product
    GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 00055415010 00055430010 00055430011 00055445010 00055445011 00055360010.A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2835-2026·2026-08-12

    Therabody Theragun G4 PRO Charger Recalled for Fire Risk

    Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.

    Product
    Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2876-2026·2026-08-12

    GE Healthcare MAC VU360 Electrocardiograph Software Recall

    GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.

    Product
    GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2843-2026·2026-08-12

    Powered Wheelchair Controller Software Recall by Pride Mobility

    Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.

    Product
    Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6 Edge 3 Stretto Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2857-2026·2026-08-12

    OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating

    OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.

    Product
    Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V526000·2026-08-12

    Nissan Recalls 2025 Altima Vehicles Due to Air Bag Fastener Defect

    Nissan is recalling 2025 Altima vehicles because incorrect mounting fasteners may prevent front passenger air bags from deploying as intended in a crash.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2854-2026·2026-08-12

    Copan WASPLab Software Recall Over Results Overwrite Issue

    Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.

    Product
    Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2852-2026·2026-08-12

    Quantum Rehab 4Front Powered Wheelchair Controller Software Recall

    Pride Mobility is recalling 1,102 Quantum Rehab 4Front powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.

    Product
    Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2875-2026·2026-08-12

    Merge OrthoPACS Imaging Workstation Recall for Patient Data Display Issue

    Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.

    Product
    Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2889-2026·2026-08-12

    Beckman Coulter MicroScan Panel Update DVD Kits Recalled

    Beckman Coulter is recalling MicroScan LabPro V5.03 Panel Update 11 DVD Kits due to incorrect algorithms that may affect antimicrobial susceptibility test results, potentially leading to false susceptibility classifications.

    Product
    REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments: - B1018-280 MicroScan autoSCAN-4 Instrument - B1018-283 MicroScan WalkAway-40 plus Instrument - B1018-284 MicroScan WalkAway-96 plus Instrument - B1018-440 DxM-1040 MicroScan Walk
    Category
    Medical Device
    Distribution
    Distributed nationwide