The Recall Desk

State

Arkansas product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18601–18625 of 78908

  • ModerateFDA (Drugs)·D-0144-2023·2023-01-25

    Akorn Recalls Moxifloxacin Ophthalmic Solution for CGMP Deviations

    Akorn, Inc. is recalling 2,563 bottles of Moxifloxacin Ophthalmic Solution nationwide due to manufacturing deviations. The recall is voluntary and affects lot 1E28A with expiration date 4/30/2023.

    Product
    Moxifloxacin Ophthalmic Solution, USP, 0.5%, 3 mL per dropper bottle, Rx only, Manufactured by: Akorn, Lake Forest, IL 60045. NDC: 17478-519-19
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0146-2023·2023-01-25

    Ofloxacin Ophthalmic Solution Recalled Nationwide for Manufacturing Quality Issues

    Akorn, Inc. is recalling Ofloxacin Ophthalmic Solution 0.3% due to manufacturing quality deviations. The recall affects 65,006 bottles distributed nationwide.

    Product
    Ofloxacin Ophthalmic Solution, USP 0.3%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045; Distributed by: MWI, Boise, ID 83705. NDC: 13985-602-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0154-2023·2023-01-25

    Drug recall: Proparacaine eye solution due to manufacturing deviations

    Akorn, Inc. is recalling Proparacaine Hydrochloride Ophthalmic Solution due to manufacturing process deviations. The voluntary recall affects 23,026 bottles distributed nationwide.

    Product
    Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL per bottle, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Distributed By: MWI Boise, ID 83705, NDC: 13985-611-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0160-2023·2023-01-25

    Triamterene and Hydrochlorothiazide Capsules Recalled for Failed Quality Specifications

    Lannett Company is recalling Triamterene and Hydrochlorothiazide Capsules nationwide because certain lots failed impurity and degradation quality specifications. Consumers taking affected lots should consult their pharmacist or physician.

    Product
    Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0167-2023·2023-01-25

    SINUVA Sinus Implant Recalled for Failed Drug Release Specification

    Intersect ENT, Inc. is recalling 9,898 pouches of SINUVA sinus implants nationwide after detecting failed drug release specifications during stability testing. The implant may not deliver the medication as intended.

    Product
    SINUVA — SINUVA (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0138-2023·2023-01-25

    Drug Recall: Erythromycin Ophthalmic Ointment Due to Manufacturing Deviations

    Akorn, Inc. recalls 1.1 million tubes of Erythromycin Ophthalmic Ointment nationwide due to manufacturing deviations. The voluntary, Class II recall was initiated by the firm.

    Product
    ERYTHROMYCIN OPHTHALMIC OINTMENT USP 0.5%, Net Weight: 3.5g (1/8 oz) per tube, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-070-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0151-2023·2023-01-25

    Prescription eye drop recall due to manufacturing compliance issues

    Akorn, Inc. is recalling Olopatadine HCl Ophthalmic Solution due to manufacturing process deviations. The nationwide voluntary recall involves 121,176 bottles distributed across the United States.

    Product
    Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 60429-957-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0155-2023·2023-01-25

    Sodium Chloride Ophthalmic Ointment Recalled for Manufacturing Deviations

    Akorn, Inc. has voluntarily recalled 524,506 tubes of Sodium Chloride Ophthalmic Ointment, USP 5%, nationwide due to Current Good Manufacturing Practice deviations.

    Product
    Sodium Chloride Ophthalmic Ointment, USP, 5%, Net Wt. 3.5 g (1/8 oz.) per tube, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-622-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V024000·2023-01-23

    Mack Recalls LRBE Electric Trucks Due to Cabin Heater Relay Fire Risk

    Mack Trucks is recalling 2019 and 2021-2023 LRBE electric trucks because a failing cabin heater relay can cause the coolant heater to overheat, increasing the risk of fire.

    Product
    MACK — MACK LRBE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V023000·2023-01-23

    Autocar Recalls Trucks Due to Parking Brake Release Risk

    Autocar is recalling specific trucks because a worn parking brake valve may cause the brake to release unexpectedly, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, WXLL, WX, XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V022000·2023-01-23

    2021 Lincoln Aviator rearview camera video output may fail

    Ford is recalling 2021 Lincoln Aviators with 360-degree camera systems because the rearview camera video may fail to display, reducing driver rear visibility and increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V017000·2023-01-23

    2022-2023 Isuzu N-Series and related commercial vehicles recalled for safety system miscalibration

    Certain 2022-2023 Isuzu, Chevrolet, and Hino commercial vehicles with improperly calibrated ABS and optional ADAS camera systems are being recalled. The miscalibration could prevent the automatic emergency braking and electronic steering control systems from functioning properly, increasing crash risk.

    Product
    ISUZU — ISUZU, HINO, CHEVROLET N-SERIES, S52, LOW CAB FORWARD 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V025000·2023-01-23

    Volvo Recalls 2019-2023 VNRE Electric Trucks Due to Fire Risk

    Volvo Trucks is recalling 2019-2023 VNRE electric trucks because a faulty cabin heater relay may cause the coolant heater to overheat, increasing the risk of fire.

    Product
    VOLVO — VOLVO VNRE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V021000·2023-01-23

    2023 Ford Bronco Sport recalled for ABS module brake defect

    Ford is recalling certain 2023 Bronco Sport vehicles because valves inside the ABS module may have been damaged during manufacturing, causing an internal leak. This can lead to unexpected brake pedal travel or unexpected movement, increasing crash risk.

    Product
    FORD — FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V018000·2023-01-23

    AUTOCAR Xpeditor Trucks: Software Error in Fuel Gauge May Cause Stalling

    Autocar is recalling 2021-2023 Xpeditor natural gas vehicles due to a software error in the instrument cluster fuel gauge. The inaccurate fuel gauge may cause the vehicle to unexpectedly run out of fuel and stall, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23V016000·2023-01-23

    2022 Subaru WRX Owner's Manual Contains Incorrect High Beam Assist Instructions

    Subaru is recalling 2022 WRX vehicles with Eyesight because the owner's manual contains incorrect instructions for adjusting the High Beam Assist function. Owners will receive a corrected manual insert by mail.

    Product
    SUBARU — SUBARU WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V014000·2023-01-20

    2021 Forest River Berkshire Coach Unintended Awning Extension Recall

    Forest River Bus is recalling certain 2021 Berkshire coaches due to a faulty retractable awning that may extend unintentionally while the vehicle is in transit. The unintended extension could distract the driver or become a road hazard, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V012000·2023-01-19

    Volvo Recalls 2023 Models Due to Brake Control Software Error

    Volvo is recalling 27,457 2023 vehicles because a software error may disable ABS, ESC, and traction control, increasing crash risk.

    Product
    VOLVO — VOLVO XC90, V90CC, XC60, XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23100·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    Weihai Juanhai Decoration Material's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn risk. About 280 units were sold on Amazon between December 2021 and May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23103·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    NewCosplay long-sleeved children's sleepwear fails to meet federal flammability standards and poses a burn hazard. The recalled garments were sold exclusively on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23104·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    About 2,140 units of NewCosplay children's sleepwear fail to meet federal flammability standards and pose a burn injury risk. The recalled garments were sold on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23097·2023-01-19

    Children's Pajama Sets Recalled for Flammability Standards Violation

    Selfie Craft Company children's pajama sets fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 38,740 units sold online and in boutiques from November 2017 through June 2022 are affected.

    Product
    Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide