The Recall Desk

State

Delaware product recalls

73,570 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
2026-10-14

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.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27151–27175 of 77008

  • SevereNHTSA·21V115000·2021-02-25

    GM Recalls 33,838 Vehicles Due to Over-Cured Continental Tires

    General Motors is recalling 33,838 vehicles equipped with over-cured Continental tires that may develop sidewall breaks or belt separation, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC EXPRESS, SIERRA 1500, SAVANA, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V119000·2021-02-25

    Vermeer Recalls 2021 BC900XL Trailers Due to Axle Bolt Issue

    Vermeer is recalling 2021 BC900XL brush chipper trailers because axle mounting bolts may not be tightened properly, increasing crash risk.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V120000·2021-02-25

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Engine Software Defect

    Daimler Trucks North America is recalling 2019-2021 Thomas Built Buses Saf-T-Liner C2 school buses because engine software may fail to limit speed or torque, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V118000·2021-02-25

    Jaguar Recalls 2019-2020 F-Pace for High Beam Indicator Software Defect

    Jaguar is recalling 2019-2020 F-Pace vehicles because the Auto High Beam system fails to display an indicator when high beams activate, potentially reducing visibility for oncoming traffic.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21089·2021-02-25

    Dr. Reddy's Recalls Prescription Blister Packages Due to Poisoning Risk

    Dr. Reddy's is recalling prescription blister packages because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Imatinib Mesylate Tablets 100 mg, Imatinib Mesylate Tablets 400 mg, Pregabalin Capsules 50 mg, Pregabalin Capsules 75 mg, Pregabalin Capsules 100 mg, Pregabalin Capsules 150 mg, Sevelamer Carbonate Tablets 800 mg, Tadalafil Tablets 5 mg and Tadalafil Tablets 20 mg
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·21722·2021-02-25

    Home Depot Recalls Wood Windsor Dining Chair Sets Due to Fall Hazard

    Home Depot is recalling StyleWell Wood Windsor Dining Chair Sets because the back can detach, posing a fall hazard. No injuries have been reported.

    Product
    StyleWell Wood Windsor Dining Chair Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V117000·2021-02-25

    Land Rover Recalls 2018-2020 Models for High Beam Indicator Defect

    Jaguar Land Rover is recalling 2018-2020 Range Rover and Discovery models because the high beam indicator may not display, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT, RANGE ROVER VELAR, DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V116000·2021-02-25

    Black Series Campers Recalls Trailers Due to Electrical Fire Risk

    Black Series Campers is recalling 2020-2021 trailers equipped with specific Curt emergency breakaway kits because a depleted battery can overload the electrical system, increasing the risk of a fire.

    Product
    BLACK SERIES CAMPERS — BLACK SERIES CAMPERS HQ21, C12, HQ22T, HQ15
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21723·2021-02-25

    deSensua Essential Oils Recalled for Non-Child-Resistant Packaging and Poisoning Risk

    MTIG Productions is recalling deSensua Wintergreen, Birch, and Pain Soother Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    deSensua Wintergreen, Birch and Pain Soother Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0255-2021·2021-02-24

    Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 1 Gal (3.78 L) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477; NDC: XXXXX-378-04, UPC # 7 501799 118837
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0253-2021·2021-02-24

    Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0256-2021·2021-02-24

    Optimus Lubricants Instant Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 275 Gal (1040 L) tank with spout dispenser, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.; UPC # 7 501799 118981
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0254-2021·2021-02-24

    Liq-E Recalls Optimus Hand Sanitizer Due to Methanol Contamination

    Liq-E S.A. De C.V. is recalling 575 drums of Optimus Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 55 Gal (208 L) drum, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col.. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.UPC # 7 501799 118998
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Donor Sets

    Combat Medical Systems is recalling 954 Fresh Whole Blood Donor Sets due to a potential bent or disconnected needle in the kit components.

    Product
    Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Blood convenience kit. The Fresh Whole Blood Doner Set contains everything needed to test for ABO/Rh compatibility and collect the whole blood from donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V107000·2021-02-24

    Lamborghini Recalls Aventador SVJ Vehicles Due to Hood Hinge Defect

    Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1113-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Transfusion Sets

    Combat Medical Systems is recalling Fresh Whole Blood Transfusion Sets due to a potential for bent or disconnected needles in the kit components.

    Product
    Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Blood convenience kit. The Fresh Whole Blood Transfusion Set contains everything needed to test for ABO/Rh compatibility and perform a fresh whole blood transfusion in a compact sealed package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1112-2021·2021-02-24

    Combat Medical Systems Recalls Low Titer Type O FWB Transfusion Sets

    Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.

    Product
    Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1110-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Collection Kits

    Combat Medical Systems is recalling 531 Valkyrie LTOWB blood collection kits due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Collection (P/N 80-820, NSN 6515016862423). Blood collection convenience kit. The Valkyrie LTOWB Collection Set includes the items needed to allow for pre-screening to identify Low Titer Type O Donors as well as collect the blood from the donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1111-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Administration Kits

    Combat Medical Systems is recalling 953 Valkyrie LTOWB Administration Sets due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood convenience kit. The Valkyrie LTOWB Administration Set contains the items needed to administer the blood to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V112000·2021-02-24

    2021 International LT Trucks Recalled for Potential Flywheel Detachment

    Certain 2021 International LT vehicles with Cummins X15 engines may have improperly torqued flywheel capscrews that could detach during operation, causing loss of drive power and risk of ejected engine parts.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1109-2021·2021-02-24

    BD 10 ml Syringes Recalled for Potential Open Seals and Sterility Compromise

    Becton Dickinson is recalling 155,200 10 ml syringes because open packaging seals may compromise sterility. The product was distributed in the US and Canada.

    Product
    BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
    Category
    Medical Device
    Distribution
    Distributed nationwide