The Recall Desk

State

Delaware product recalls

73,366 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,438
Critical
477
Severe
1,110
Most recent
2026-09-23

Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,110 (32%) are Severe.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19376–19400 of 76804

  • ModerateFDA (Devices)·Z-0220-2023·2022-11-16

    Diagnostic Calibrator Kit Recalled for Software Defect Affecting System Calibration

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Calibrator Kit 9 due to incorrect calibration software (DRVs 6194-6200) that prevents laboratory systems from successfully calibrating, causing delayed test results.

    Product
    VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS PHYT Slides For in vitro diagnostic use only. Product Code: 8568040 . VITROS Chemistry Products Calibrator Kit 9 is used to calibrate VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V845000·2022-11-15

    Nova Bus Recalls LFS Models Due to Steering Fastener Risk

    Nova Bus is recalling 2018-2022 LFS and 2018-2021 LFS Artic buses because steering fasteners may loosen, causing loss of steering and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V844000·2022-11-15

    Tesla Model Y and Model 3 vehicles recalled for taillight failures

    Tesla is recalling certain 2023 Model 3 and 2020-2023 Model Y vehicles because taillights may intermittently fail to illuminate. A failed taillight reduces vehicle visibility and increases crash risk; Tesla is providing a free over-the-air software update.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V843000·2022-11-15

    2021-2023 Tesla Model X Passenger Airbag Deployment Defect

    Tesla is recalling certain 2021-2023 Model X vehicles because a software calibration error in the restraint control module may prevent the front passenger airbag from deploying correctly during crashes, increasing injury risk.

    Product
    TESLA — TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V840000·2022-11-14

    Thomas Built Buses Recalls Minotour School Buses for Seat Barrier Defect

    Daimler Trucks North America is recalling 2021-2023 Thomas Built Buses Minotour school buses because the forward seat barrier may not provide sufficient protection, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V836000·2022-11-11

    Kia Recalls 2017-2018 Niro Hybrids for Fire Risk

    Kia is recalling 2017-2018 Niro hybrid vehicles because a faulty relay may cause rear seats to overheat, increasing the risk of a fire.

    Product
    KIA — KIA NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V837000·2022-11-11

    2022 Indian Chief Bobber fuel pump failure recall

    Indian is recalling 2021-2022 Scout and Chief motorcycles for fuel pump failure that may cause engine stall while riding. Dealers will replace the fuel pump and seal free of charge.

    Product
    INDIAN — INDIAN SUPER CHIEF LIMITED, SCOUT SIXTY, CHIEF DARK HORSE, SCOUT ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V838000·2022-11-10

    Subaru Recalls 2009-2013 Forester Vehicles for Seat Belt Defect

    Subaru is recalling 2009-2013 Forester vehicles because the front seat belt force-limiter may not operate correctly in a crash, increasing injury risk.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23040·2022-11-10

    Generac and DR Portable Generators Recalled for Finger Amputation Risk

    Generac and DR 6500- and 8000-watt portable generators are being recalled because an unlocked handle can pinch and amputate fingers. The firm has received 37 injury reports, including 24 finger amputations.

    Product
    Generac® and DR® 6500 Watt and 8000-Watt portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23042·2022-11-10

    Mockingbird Single-to-Double Strollers Recalled Due to Fall Hazard

    Mockingbird Single-to-Double Strollers may have cracks in the frame that pose a fall risk to children. The manufacturer has received 138 reports of frame cracks, including 8 injuries, and is offering free frame reinforcement kits.

    Product
    Mockingbird Single-to-Double Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V834000·2022-11-10

    2023 International MV vehicles recalled for loose wheel hub risk

    Navistar is recalling 2023 International MV vehicles because locking clips on the wheel hub retaining nut may be damaged, causing the wheel hub to loosen and separate from the axle housing, which increases crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V835000·2022-11-10

    RAM 2500 and 3500 transmission fluid leak increases fire risk

    RAM is recalling certain 2500 and 3500 vehicles due to transmission fluid leaks that could cause fires. Dealers will replace the affected components at no cost.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23041·2022-11-10

    Hunter Fan Recalls Five Lighting Collections Due to Electric Shock Hazard

    Hunter Fan Company is recalling approximately 2,600 light fixtures from five collections because internal wires can become damaged, posing an electric shock hazard. Consumers should stop using the products immediately and contact Hunter for a full refund.

    Product
    Hunter branded Devon Park, Astwood, Highland Hill, Kerrison and Van Nuys light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0153-2023·2022-11-09

    CritiCool Thermoregulation Device Recalled Due to Pump Failure

    The CritiCool thermoregulation device may experience premature pump failure leading to a HALT 4 error from which the device cannot recover, potentially delaying treatment. One death has been reported.

    Product
    CritiCool, thermoregulation device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V832000·2022-11-09

    Motorhome interior step tread may detach, increasing fall injury risk

    Holiday Rambler and Fleetwood motorhomes (2022–2023) have interior step treads that may be improperly secured and can detach when stepped on, creating a fall hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD INVICTA, VACATIONER, BOUNDER, FORTIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0158-2023·2022-11-09

    Surgical Cataract Pack Recalled Due to Compromised Sterile Packaging

    Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0172-2023·2022-11-09

    BD Trucount Tubes Recalled Due to Partial Label Detachment Causing Operational Failures

    Becton Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together in pouches or fail when used with automated loaders. No illnesses have been reported.

    Product
    BD Trucount Tubes (Cat. No. 663028), used for determining absolute counts of leukocytes in blood. BD Trucount Tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount Tubes can be used with the…
    Category
    Medical Device
    Distribution
    43 states
  • HighFDA (Devices)·Z-0170-2023·2022-11-09

    Aneurysm Embolization System Detachment Controller Recalled for Manufacturing Defect

    MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.

    Product
    WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm Embolization System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0157-2023·2022-11-09

    Bausch + Lomb Ophthalmic Surgical Kits Recalled for Sterile Packaging Defect

    Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.

    Product
    BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0106-2023·2022-11-09

    Bella Cucina Walnut Sage Pesto recalled for undeclared milk allergen

    Bella Cucina Artful Food is recalling Walnut Sage Pesto because milk is present in the product but not declared on the label. Consumers allergic to milk should not consume this product.

    Product
    Bella Cucina Artful Food Walnut Sage Pesto Net Wt. 6 oz (169g) glass jar, UPC 6 19193 00041 6 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
    Category
    Food
    Distribution
    45 states
  • HighFDA (Devices)·Z-0171-2023·2022-11-09

    BD Trucount Tubes for Blood Testing Recall Due to Label Detachment

    Becton, Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together or create automation errors. The defect stems from an adhesive supplier change and affects 52,570 units.

    Product
    BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount tubes can be used with the…
    Category
    Medical Device
    Distribution
    43 states