The Recall Desk

State

Arkansas product recalls

73,570 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.

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26251–26275 of 79113

  • SevereFDA (Drugs)·D-0399-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because they contain less active ingredient than labeled. The recall covers bottles distributed nationwide.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V418000·2021-06-02

    Stonebrooke RAM 5500 Recalled for Rear Brake Fluid Leak Risk

    Stonebrooke is recalling one 2019 RAM 5500 because the rear brake line can wear and leak, increasing crash risk.

    Product
    STONEBROOKE EQUIPMENT — STONEBROOKE EQUIPMENT RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0626-2021·2021-06-02

    Brill Inc Recalls Chocolate Chip Cookies for Potential Foreign Objects

    Brill Inc is recalling specific batches of 12-inch chocolate chip message cookies due to a potential risk of containing small foreign objects.

    Product
    10194739 TranSmart" 12 INCH CHOCOLATE CHIP MESSAGE COOKIE 24/24 OUNCE CHOCOLATE CHIP COOKIES IN BAKEABLE PLASTIC PANS WITH DOMES KEEP FROZEN AT 0¿F OR BELOW Net weight: 36 lb (16.33 kg) (24 x 24 oz (680g))
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V415000·2021-06-02

    Genesis Supreme Wanderer and Vortex RV Trailers Recalled for Cooking Stove Gas Leak

    Genesis Supreme RV is recalling certain 2020-2021 Wanderer and Vortex trailers with Dometic cooking stoves. An overtightened saddle valve securing bolt can damage the seal and cause a gas leak, increasing fire risk.

    Product
    GENESIS SUPREME — GENESIS SUPREME VORTEX, WANDERER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E049000·2021-06-02

    Adventurer Truck Campers Recalled for Potential Gas Leak from Dometic Stoves

    Adventurer LP is recalling specific truck campers equipped with Dometic stoves because a saddle valve bolt may be overtightened, causing a gas leak that increases fire risk.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2021·2021-06-02

    Radiometer Recalls PICO70 Arterial Blood Samplers Due to Sterile Barrier Breach

    Radiometer is recalling PICO70 Arterial Blood Samplers because a sterile barrier breach was found during testing, posing a risk of bacterial infection.

    Product
    PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler product line for collection of arterial samples for pH, blood gas, oximetry, electrolyte and metabolite analysis. Model Number/Product Description: 956-518…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2021·2021-06-02

    Welch Allyn GS777 Wall Transformer Recalled for Electrical Shock Risk

    Welch Allyn is recalling GS777 Wall Transformers due to a potential risk of fluid ingress causing electrical shorts and shock.

    Product
    GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V413000·2021-06-02

    2021 Volkswagen ID.4 recalled for incorrect headlight aiming caps

    Volkswagen is recalling certain 2021 ID.4 vehicles because headlight aiming caps were installed on the vertical adjustment instead of the horizontal adjustment. This defect can increase glare and reduce visibility, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2021·2021-06-02

    Brill Inc Recalls Jumbo Chocolate Chip Cookies Due to Foreign Objects

    Brill Inc is recalling Jumbo Chocolate Chip Cookies nationwide because they may contain small foreign objects.

    Product
    10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN Net weight: 17.04 lb (7.73 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2021·2021-06-02

    Beckman Coulter Access SARS-CoV-2 Antigen Recalled for False Negative Risk

    Beckman Coulter is recalling Access SARS-CoV-2 Antigen test kits because specimens stored in certain conditions may yield false negative results.

    Product
    Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d, 3.10 mL, R1e
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V416000·2021-06-02

    Mack 2021-2022 trucks recalled for hubcap separation hazard

    Mack Trucks is recalling 307 certain 2021-2022 Granite, Pinnacle, and Anthem commercial trucks due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard and increasing crash risk.

    Product
    MACK — MACK ANTHEM (AN), GRANITE (GR), PINNACLE (CHU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V410000·2021-06-02

    Mercedes-Benz Sprinter Recall for Swivel Seat Wiring Harness Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans with swivel seats because incorrect wiring harness routing may damage the seat air bag system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2021·2021-06-02

    Pentax Medical Video Duodenoscope Recalled for Distal End Cap Detachment Risk

    Pentax of America Inc. is recalling 108 Pentax Medical Video Duodenoscopes because the distal end cap may detach during procedures, posing risks of injury or aspiration.

    Product
    Pentax Medical Video Duodenoscope - Product Usage: intended to be used with endoscopic devices and other ancillary equipment to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract, Model Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2021·2021-06-02

    Welch Allyn ProBP 3400 Digital Blood Pressure Device Recall

    Welch Allyn is recalling ProBP 3400 Digital Blood Pressure Devices due to a risk of fluid ingress causing electrical shorts and potential shock.

    Product
    ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: ProBP 3400 automatically measures systolic and diastolic pressure (excluding neonates) and pulse rate, as well as calculates Mean Arterial Pressure (MAP).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1687-2021·2021-06-02

    James Leckey MyWay Walker Chassis Recalled Due to Weld Failure

    James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.

    Product
    MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2021·2021-06-02

    Dentech Corp. Recalls Rubber Dam Clamps Due to Possible Breakage

    Dentech Corp. is recalling 87,842 units of KSK Rubber Dam Clamps because they may break during use. The recall covers units distributed in the US and worldwide.

    Product
    Rubber Dam Clamp, KSK - Product Usage: used for prevention of contamination by saliva and moisture prevention during dental treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V411000·2021-06-02

    Mercedes-Benz and Freightliner Sprinter Recalled for Rearview Camera Software Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because a software defect may cause the rearview camera image to fail to display.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1671-2021·2021-06-02

    Philips IntelliVue MX40 Patient Monitor Recalled for Manufacturing Defects

    Philips is recalling three IntelliVue MX40 patient monitors because manufacturing process failures may have resulted in defective devices.

    Product
    IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product Usage: Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06022021·2021-06-02

    USDA Issues Public Health Alert for Raw Breaded Stuffed Chicken Products

    USDA FSIS issued a public health alert for frozen raw breaded stuffed chicken products due to a Salmonella Enteritidis illness cluster. Consumers are advised to cook products to 165 F.

    Product
    FSIS Issues Public Health Alert for Frozen Raw Breaded Stuffed Chicken Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V417000·2021-06-02

    Volvo Trucks recalls 2021-2022 vehicles for hubcap separation hazard

    Volvo Trucks is recalling certain 2021-2022 VAH, VDH, VNL, and VNR vehicles due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard. Dealers will remove the hubcap free of charge.

    Product
    VOLVO — VOLVO VNL, VAH, VHD, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1679-2021·2021-06-02

    Nobel Biocare Implant Crown Recalled for Manufacturing Specification Defects

    Nobel Biocare Procera LLC is recalling specific implant crown units because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77363
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1675-2021·2021-06-02

    Roche Recalls Iron Gen 2 Reagent Cassettes Due to Discrepant Results

    Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.

    Product
    IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for the quantitative determination of iron in human serum and plasma on Roche/Hitachi cobas c and cobas Integra systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1681-2021·2021-06-02

    Nobel Biocare Procera LLC Recalls Implant Crowns Not Manufactured to Specification

    Nobel Biocare Procera LLC is recalling specific implant crowns because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77387
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1674-2021·2021-06-02

    Siemens Centaur Syphilis Assay Recalled for Potential Carryover Interference

    Siemens Healthcare Diagnostics is recalling the Centaur Syphilis Assay-SYP Kit due to potential carryover into other assays on specific systems.

    Product
    Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualitative determination of antibodies to Treponema pallidum in human serum or plasma using the ADVIA Centaur XP/XPT System and ADVIA Centaur CP Systems, SMN:10492493
    Category
    Medical Device
    Distribution
    Distributed nationwide