The Recall Desk

State

Arkansas product recalls

73,376 recalls have nationwide distribution and so reach Arkansas. 5,542 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total
5,542
Critical
1,029
Severe
1,446
Most recent
2026-09-23

Of the 5,542 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 5,542 recalls whose distribution notice names Arkansas specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19026–19050 of 78918

  • ModerateFDA (Devices)·Z-0467-2023·2022-12-21

    NexGen Option Stemmed Tibial Knee Component Recalled for Higher Revision Rates

    Zimmer Biomet is recalling NexGen Option Stemmed Tibial knee components (2,092 units) due to clinically significant higher revision rates when used with specific femoral components. The voluntary recall prevents future implantation with these problematic combinations.

    Product
    NexGen Option Stemmed Tibial Component Size 4, Item Number 00-5986-037-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0716-2023·2022-12-21

    Siemens Allergen Test Kit Recall: False Positive Mold Results

    Siemens is recalling IMMULITE 2000 allergen test kits that may produce false positive results for mold allergies in both quality control and patient samples.

    Product
    IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)- US. Siemens Material Number (SMN): 10708840 For in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers for the quantitative measurement of allergen-specific IgE in human serum, as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0496-2023·2022-12-21

    Dental Procedure Trays Recalled for Incomplete Outer Bag Seal

    STRADIS HEALTHCARE dental procedure trays may have incompletely sealed outer bags that could compromise sterility. The recall affects units distributed nationwide in the US and Canada.

    Product
    STRADIS HEALTHCARE, Custom Pack, Item No.41213ATCP, dental
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2023·2022-12-21

    FDA recalls Neuroquell Calendula Oil homeopathic drug for manufacturing deviations

    The FDA has recalled Neuroquell Calendula Oil, a homeopathic drug, due to manufacturing practice violations. The voluntary recall affected 51 bottles distributed nationwide and in Australia.

    Product
    Neuroquell, A Homeopathic Drug, Calendula Oil, packaged in1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0081-2023·2022-12-21

    Drug Neuroquell Plus Calendula Oil Recalled for Manufacturing Deviations

    Neuroquell Plus, a homeopathic calendula oil drug, has been voluntarily recalled due to current good manufacturing practice (cGMP) deviations. The recall affects 461 bottles distributed nationwide and in Australia.

    Product
    Neuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6 mL) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0083-2023·2022-12-21

    Drug Recall: ProSirona Homeopathic Calendula Oil Manufacturing Deviations

    ProSirona Homeopathic Calendula Oil (Lot B-02) is being recalled because the manufacturer failed to follow Current Good Manufacturing Practice standards. The voluntary recall affects products distributed nationwide and in Australia.

    Product
    ProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by: Endometriosis Assoc. Inc. (International), Mfg. by Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-712-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V943000·2022-12-20

    New Flyer Transit Buses Recalled for Steering Column Defect

    New Flyer is recalling 746 transit buses because a loose steering column connection may cause loss of steering, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XT40, XDE35, XN40, XT60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V942000·2022-12-19

    2023 BMW X5 driver seat backrest fastener defect recall

    BMW is recalling certain 2023 X5 models because one of four bolts connecting the driver's seat backrest to the frame may not have been correctly installed, potentially preventing proper occupant restraint during a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V939000·2022-12-16

    Peterbilt 320 and 520 Refuse Trucks Recalled for Suspension Defect

    PACCAR is recalling 2015-2023 Peterbilt 320 and 520 refuse trucks because suspension brackets may fail, causing axle instability and increasing crash risk.

    Product
    PETERBILT — PETERBILT 320, 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V934000·2022-12-16

    Lightning eMotors Recalls FE4 Vehicles for Battery Power Loss Risk

    Lightning eMotors is recalling 2021-2022 FE4-129 vehicles because the high-voltage battery may lose traction power or fail to start, increasing crash risk.

    Product
    LIGHTNING EMOTORS — LIGHTNING EMOTORS FE4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V936000·2022-12-16

    Mercedes-Benz Recalls GLE and GLS Models for Steering Screw Defect

    Mercedes-Benz is recalling 2021-2022 GLE and GLS vehicles because a steering coupling locking screw may loosen, potentially causing a loss of steering control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE63, GLS 450 4MATIC, AMG GLE53, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V937000·2022-12-16

    Mercedes-Benz Recalls 2022 AMG G63 Due to Rear Axle Defect

    Mercedes-Benz is recalling 278 2022 AMG G63 vehicles because the rear axle differential housing may crack or break, potentially causing loss of control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V941000·2022-12-16

    Hyundai Recalls 2021 Kona Electric Vehicles Due to EPCU Coolant Leak Risk

    Hyundai is recalling 2021 Kona Electric vehicles because a defective Electric Power Control Unit may leak coolant, potentially causing a loss of drive power and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI KONA ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V935000·2022-12-16

    Mercedes-Benz Recalls One 2022 S 500 for Dashboard Attachment Defect

    Mercedes-Benz is recalling one 2022 S 500 vehicle because the dashboard may be insufficiently attached, which can result in improper front passenger air bag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V940000·2022-12-16

    Peterbilt 579 Hood Mirror Assemblies May Break and Fall

    PACCAR is recalling certain 2022–2023 Peterbilt 579 vehicles because the molded hood mirror assemblies may break at the pivot joint and fall into the roadway, creating a road hazard.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V938000·2022-12-16

    Mercedes-Benz Recalls 2019 AMG GT Models for Center Console Defect

    Mercedes-Benz is recalling 2019 AMG GT53 and GT63 vehicles because the center console may unlatch during a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT 63, AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·044-2022·2022-12-15

    Mountain View Packaging Recalls Frozen Crispy Chicken Entrée for Undeclared Shrimp

    Mountain View Packaging is recalling frozen Crispy Chicken with Almonds entrée due to undeclared shrimp, a known allergen. No adverse reactions have been reported.

    Product
    Mountain View Packaging, LLC — Mountain View Packaging, LLC, Recalls Frozen Ready-To-Eat Crispy Chicken with Almonds Entrée Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23716·2022-12-15

    Gyroor C3 E-Bikes Recalled for Fire and Burn Hazards

    Gyroor C3 e-bikes are recalled because the battery pack can ignite, creating fire and burn hazards. Gyroor has received reports of battery packs igniting and injuries requiring medical treatment, including burns and smoke inhalation.

    Product
    Gyroor C3 e-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V930000·2022-12-15

    Chevrolet Bolt EV Pretensioner Exhaust Fire Risk Recall

    General Motors recalls 2017-2023 Chevrolet Bolt EV vehicles. After a crash with pretensioner deployment, pretensioner exhaust may ignite carpet near the B-pillar, creating a fire hazard.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E100000·2022-12-15

    Ridewell 266 Suspension Brake Pad Retaining Clip Recall

    Ridewell is recalling certain 266 Suspensions with Haldex Air Disc Brakes because a retaining clip may detach, reducing brake performance or causing a flat tire.

    Product
    SERVICE BRAKES, AIR:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23070·2022-12-15

    Samnyte Tattoo Numbing Cream Recalled for Non-Child-Resistant Packaging

    Samnyte Tattoo Numbing Cream is recalled because its packaging does not meet child-resistant requirements under federal law. The product contains lidocaine and poses a poisoning risk if ingested by young children.

    Product
    Samnyte Tattoo Numbing Creams
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23072·2022-12-15

    Good Matters Three-Wick Candles Recalled for Fire and Laceration Hazards

    About 30,100 Good Matters three-wick candles are being recalled because the candles can burn at higher than usual temperatures, causing glass jars to break and posing fire and laceration injury risks.

    Product
    Good Matters Three-Wick Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23069·2022-12-15

    Rosso Motors Youth ATVs Recalled for Federal Safety Standard Violations

    Rosso Motors is recalling approximately 2,800 eQuad X and eQuad Q youth ATVs sold online from June 2019 through April 2021 because they violate federal safety standards and pose a risk of serious injury or death.

    Product
    Rosso Motors eQuad X and eQuad Q Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide