The Recall Desk

State

Oklahoma product recalls

20,199 recalls have nationwide distribution and so reach Oklahoma. 0 additional recalls listed Oklahoma specifically in their distribution scope.

About recalls in Oklahoma

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Oklahoma consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

8751–8775 of 20199

  • CriticalCPSC·24265·2024-06-13

    Magnetic Chess Games Recalled for High-Powered Magnet Ingestion Hazard

    About 2,600 magnetic chess games with 20 magnet pieces sold on Temu.com from December 2023 through February 2024 are recalled because the magnets violate federal toy magnet regulations and pose a serious ingestion hazard.

    Product
    1 Set Puzzle "Magnetic", "Magnetism", or "Magnetism Intelligence Strategy Game" Magnetic Battle Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24262·2024-06-13

    Southern Telecom Recalls Lomi Roll-On Waxing Kits for Fire and Shock Hazards

    Southern Telecom is recalling about 19,500 Lomi Roll-On Waxing Kits because the power cord can overheat and short circuit, creating fire, burn, and electrical shock hazards. Two consumers suffered burns and one incident of property damage has been reported.

    Product
    Lomi Roll-On Waxing Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24260·2024-06-13

    Daikin Air Conditioning and Heat Pump Units Recalled for Fire Hazard

    Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.

    Product
    Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24264·2024-06-13

    Bambu Lab A1 3D Printers Recalled for Electric Shock and Fire Hazards

    Bambu Lab is recalling about 12,800 A1 3D printers sold between December 2023 and January 2024 due to damaged or bent heatbed cables that can short-circuit, spark, or burn through insulation, creating electric shock and fire risks. No injuries have been reported.

    Product
    Bambu Lab A1 3D printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24266·2024-06-13

    Beaumont Plus ST Bicycles with Disc Brakes Recalled for Brake Failure Risk

    Retrospec is recalling about 530 Beaumont Plus ST bicycles with disc brakes because the front brake rotor and pads can become misaligned, potentially causing brake failure and crashes. No injuries have been reported.

    Product
    Beaumont Plus ST Bikes with disc brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24261·2024-06-13

    Black Diamond Neve Strap Crampons Recalled Due to Fall Hazard

    Black Diamond Equipment is recalling Neve Strap Crampons and Accessory Kits because screws connecting the heel cup to the crampon can loosen, causing the heel cup to detach and creating a fall hazard. The firm has received three reports of incidents but no injuries have been reported.

    Product
    Neve Strap Crampons and Accessory Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24263·2024-06-13

    Nap Queen Sleep Victoria Hybrid Mattresses Recalled for Fire Hazard

    Adven Group is recalling approximately 117,200 Nap Queen Sleep Victoria Hybrid Mattresses sold nationwide from February 2020 through October 2023 because they violate federal flammability regulations, posing a fire hazard.

    Product
    Nap Queen Sleep Victoria Hybrid Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1920-2024·2024-06-12

    Pediatric Patient Return Electrode Recalled for Reported Patient Burns

    Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.

    Product
    MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V858000·2024-06-12

    Fuel pump failure recall for 2013-2023 Honda and Acura vehicles

    Honda is recalling certain 2013-2023 Honda Accord, Civic, CR-V, HR-V, Odyssey, Pilot, Ridgeline and Acura ILX, MDX, RDX, RLX, TLX vehicles because the fuel pump inside the fuel tank may fail, potentially causing engine stall while driving and increasing crash risk.

    Product
    ACURA — 2020 ACURA RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1878-2024·2024-06-12

    Intra-Aortic Balloon Catheter Kit Recalled for Inflation and Structural Defects

    Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.

    Product
    Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1880-2024·2024-06-12

    Arrow Ultra 8 Intra-Aortic Balloon Catheter Kit Recalled for Inflation Defect

    The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.

    Product
    Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-05840-U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1879-2024·2024-06-12

    Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled for Device Malfunction

    Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.

    Product
    Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF IAB-06850-U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1938-2024·2024-06-12

    Medline Luer Slip Syringes Recalled for Inaccurate Volume Delivery

    Medline Industries is recalling over 5 million Luer Slip disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity range. This poses a risk to patient health.

    Product
    MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1949-2024·2024-06-12

    Medical device recall: HA FlexTrak patient transport trolley oil leak hazard

    Philips is recalling the HA FlexTrak patient transport trolley due to potential oil leaks from the hydraulic system that create slipping and falling hazards. Approximately 100 units have been distributed worldwide.

    Product
    HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006412
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1954-2024·2024-06-12

    ADVANTA VXT vascular graft recalled for slider rod separation

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to complaints of separation between the slider rod and swivel core, which could affect proper device function.

    Product
    ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1944-2024·2024-06-12

    Alaris Pump Infusion Set Drip Chamber May Detach During Use

    A defective drip chamber in the Alaris Pump Infusion Set may detach from the tubing, potentially delaying treatment or causing unintended exposure to medications. BD is recalling approximately 11,300 units distributed across the US and Canada.

    Product
    Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1971-2024·2024-06-12

    ADVANTA VXT Vascular Grafts Recalled for Slider Rod Separation

    Atrium Medical is recalling 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the slider rod from the swivel core, with a gap observed between the components.

    Product
    ADVANTA VXT, 6X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0535-2024·2024-06-12

    FDA Recalls Rizatriptan Benzoate Tablets for Manufacturing Impurity

    Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate 10mg tablets nationwide due to N-nitroso impurity levels exceeding FDA acceptable limits, affecting 13,296 cartons.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1975-2024·2024-06-12

    ADVANTA VXT vascular graft recalled for swivel rod separation

    Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of swivel rod separation from the swivel core. Affected units distributed worldwide; healthcare providers should evaluate appropriate management.

    Product
    ADVANTA VXT, 6X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2015-2024·2024-06-12

    FLIXENE Vascular Graft Slider Rod Separation Defect Recall

    Atrium Medical Corporation has recalled FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core and a notable gap between the pieces.

    Product
    FLIXENE, 4-7X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1984-2024·2024-06-12

    Vascular graft separation reported in ADVANTA VXT medical devices

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Approximately 53,308 units have been affected worldwide.

    Product
    ADVANTA VXT, 7X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0534-2024·2024-06-12

    Prescription migraine drug recalled for manufacturing impurity above FDA limit

    Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate tablets for exceeding FDA acceptable limits of N-Nitroso Desmethyl Rizatriptan impurity. The recall affects 2,400 cartons distributed nationwide.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1940-2024·2024-06-12

    Synchro SELECT Guidewires may have PTFE coating damage

    Stryker Neurovascular recalls certain lots of Synchro SELECT Guidewires due to PTFE coating damage that may occur when using a backloading technique. The damage is caused by sharper-than-intended edges on older introducer versions.

    Product
    The Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014in. The guidewires are compatible with existing microcatheters used in common procedures s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1988-2024·2024-06-12

    Vascular graft component separation risk: ADVANTA VXT slider rod defect

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of separation between the Slider GDS Swivel Rod and Swivel Core, potentially affecting device functionality.

    Product
    ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1976-2024·2024-06-12

    Vascular graft device recalled for swivel component separation

    Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of the Slider GDS Swivel Rod separating from the Swivel Core. The internal component separation could compromise device function.

    Product
    ADVANTA VXT, 7X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide