The Recall Desk

State

Arkansas product recalls

73,566 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total
5,543
Critical
1,029
Severe
1,446
Most recent
2026-10-14

Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,446 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25501–25525 of 79109

  • SevereCPSC·21175·2021-08-04

    LG Energy Solution Recalls RESU10H Home Batteries for Fire Hazard

    LG Energy Solution Michigan is recalling about 10,000 RESU10H lithium-ion residential energy storage batteries because they can overheat and catch fire, emitting harmful smoke. The firm has received five reports of batteries smoking and catching fire, resulting in property damage and one injury.

    Product
    LG Chem "RESU10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2021·2021-08-04

    Eat Gangster Oatmeal Cookie Mix Recalled for Salmonella Contamination

    Eat Gangster Oatmeal Schmoatmeal Cookie Mix has been recalled due to potential Salmonella contamination in tigernut flour, an ingredient used in the product. The affected 8.5 oz bags were distributed nationwide.

    Product
    Eat GANGSTER, Oatmeal Schmoatmeal Cookie Mix, 8.5 Oz, Eat GANGSTER LLC, Wichita, KS, UPC 0 51497 13952 0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0802-2021·2021-08-04

    Randall Navy Beans recalled due to non-functioning temperature devices

    Randall Foods is recalling Randall Navy Beans in 48 oz and 15.4 oz glass jars due to lack of functioning temperature indicating devices in retorts during processing.

    Product
    RANDALL NAVY BEANS 48OZ glass jars UPC 070095000506; RANDALL NAVY BEANS 15.4OZ glass jars UPC 070095000537
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0798-2021·2021-08-04

    Randall and Hurst's Great Northern Beans Recalled for Temperature Device Failure

    Randall Foods, Inc. is recalling Randall and Hurst's brand Great Northern Beans due to non-functioning temperature indicating devices in the canning equipment, which could allow underprocessed product to reach consumers.

    Product
    RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC 070095000117; RANDALL GREAT NORTHERN BEANS 15.4OZ glass jar UPC 070095000131; RANDALL ORGANIC GREAT NORTHERN BEANS 48OZ glass jar UPC 070095005105; Hurst's Fully Cooked…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-2005-2021·2021-08-04

    Recirculator 8.0s Disposable Lavage Kit recalled for potential aluminum ion release

    Eight Medical International BV is recalling the Recirculator 8.0s Disposable Lavage Kit due to potential aluminum ion release during warming therapy that may expose patients under certain use conditions.

    Product
    Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperthermic Perfusion System intended to raise the temperature of the thoracic or peritoneal cavity to a target temperature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0805-2021·2021-08-04

    Randall Ultimate 4-Bean Mix Recalled for Lack of Temperature Indicators

    Randall Foods, Inc. is recalling Randall Ultimate 4-Bean Mix in 48 oz glass jars due to non-functioning temperature indicating devices in retorts used during processing, which may affect proper sterilization.

    Product
    RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0799-2021·2021-08-04

    Randall Pinto Beans Recall Due to Temperature Control Defect

    Randall Foods, Inc. is recalling Randall Pinto Beans in three sizes (48oz, 24oz, and 15.4oz glass jars) distributed across 22 states due to lack of functioning temperature-indicating devices in retorts used during processing.

    Product
    RANDALL PINTO BEANS 48OZ glass jars UPC 070095000209; RANDALL PINTO BEANS 24OZ glass jars UPC 070095000216; RANDALL PINTO BEANS 15.4OZ glass jars UPC 070095000230
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0801-2021·2021-08-04

    Randall Kidney Beans Recall for Faulty Temperature Devices

    Randall Foods, Inc. is recalling Randall Kidney Beans in three sizes due to non-functioning temperature indicating devices in retorts, which may affect proper heat sterilization during processing.

    Product
    RANDALL KIDNEY BEANS 48OZ glass jars UPC 070095000308; RANDALL KIDNEY BEANS 24OZ glass jars UPC 070095000315; RANDALL KIDNEY BEANS 15.4OZ glass jars UPC 070095000339
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-2161-2021·2021-08-04

    OEC Elite Mobile C-Arm Recalled for Battery Depletion

    GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.

    Product
    OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2021·2021-08-04

    CooperVision Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling MEDIFLEX ELITE 1 DAY TORIC daily disposable contact lenses (lot W0106167) due to misaligned axis marks that can cause blurred vision.

    Product
    MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V608000·2021-08-04

    2021 Porsche Taycan Seat Belt Retractor Defect May Prevent Child Restraint Securing

    Porsche is recalling certain 2021 Taycan models because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly during a crash.

    Product
    PORSCHE — PORSCHE PANAMERA GTS, 911, TAYCAN, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21174·2021-08-04

    Two Million Dehumidifiers Recalled for Fire and Burn Hazards

    About 2 million dehumidifiers manufactured by New Widetech under multiple brand names are recalled because they can overheat and catch fire, posing fire and burn hazards. Consumers should stop using them immediately.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2150-2021·2021-08-04

    Contact lens recall: misaligned axis mark may cause blurred vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that may cause blurred vision. The recall affects 450 lenses distributed across select U.S. states and multiple countries.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2021·2021-08-04

    CLARITI 1 DAY TORIC Contact Lenses Recalled Due to Axis Mark Misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected patients should discontinue use and contact their eye care provider.

    Product
    CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0804-2021·2021-08-04

    Randall Garbanzo Beans Recall: Defective Temperature Monitoring Devices

    Randall Foods is recalling Randall Garbanzo Beans in 24oz and 15.4oz glass jars due to non-functioning temperature indicating devices in retorts, which may affect proper food safety processing.

    Product
    RANDALL GARBANZO BEANS 24OZ glass jars UPC 070095000711; RANDALL GARBANZO BEANS 15.4OZ glass jars UPC 070095000735
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-2144-2021·2021-08-04

    Contact Lens Axis Mark Misalignment May Cause Blurred Vision

    CooperVision's AQUATECH PLUS 1 DAY TORIC contact lenses (lot R0121629) have misaligned axis marks that may cause blurred vision in patients.

    Product
    AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2163-2021·2021-08-04

    Coaxial Interventional Needles recalled for potential sterilization failure

    Coaxial Interventional Needles from INNOVATIVE TOMOGRAPHY PRODUCT GMBH may not be properly sterilized. Multiple lot numbers are affected and should not be used.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21E071000·2021-08-04

    Enerco Propane Regulators Recalled Due to Fire Risk

    Enerco Group is recalling specific propane regulators that may fail, causing excessive gas pressure and increased fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis mark misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC daily disposable contact lenses due to misaligned axis marks that can cause blurred vision. Affected lenses in lot U0108833 were distributed in seven US states and internationally.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V609000·2021-08-04

    Peterbilt 220 Recall for Stator Assembly Wire Crimping Defect

    PACCAR is recalling 2020 Peterbilt 220 trucks with Meritor 14Xe ePowertrains due to insufficiently crimped stator wires that may cause overheating and loss of drive power.

    Product
    PETERBILT — PETERBILT 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2021·2021-08-04

    Medical inflation device recalled due to handle separation risk

    Merit Medical Systems is recalling basixALPHA Inflation Devices due to a design flaw where the syringe handle can separate when withdrawn, affecting device functionality.

    Product
    basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or other interventional device, and to measure the pressure within the balloon.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V604000·2021-08-04

    Newmar Motorhomes Recalled for Potential Fuel Leak and Fire Risk

    Newmar Corporation is recalling certain 2021-2022 motorhomes (New Aire, Ventana, and Dutch Star) with Cummins L9 diesel engines due to potential fuel leaks that could increase fire risk. Affected owners should contact Newmar customer service at 1-800-731-8300 for free fuel hose replacement.

    Product
    NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2164-2021·2021-08-04

    Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.

    Product
    Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V603000·2021-08-04

    Lamborghini Recalls 2021 Urus for Rear Seat Belt Retract Defect

    Lamborghini is recalling 2021 Urus vehicles because middle-rear seat belt retractors may deactivate early, preventing child restraints from securing properly.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide