The Recall Desk

State

Delaware product recalls

73,213 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
939
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 939 (27%) are Severe.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15476–15500 of 76651

  • HighFDA (Devices)·Z-2234-2023·2023-08-02

    Laser fiber medical devices recalled for potential burn injury hazard

    Boston Scientific recalls Flexiva Pulse laser fibers due to manufacturing defects that can cause fiber connector overheating and potential burns if touched. Affects 280 units in US and Canada.

    Product
    Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy 5-pack UPN: M006L8406961
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2023·2023-08-02

    Laser Fiber Devices May Overheat and Cause Burns During Use

    Boston Scientific is recalling Flexiva Pulse 242 laser fibers due to manufacturing defects that may cause the fiber connector to overheat and cause burn injuries. The recall affects 1,245 units distributed in the US and Canada.

    Product
    Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy. 5-pack UPN: M006L8405961
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0935-2023·2023-08-02

    Oxacillin Injectable Recalled for Failure to Assure Sterility

    Sagent Pharmaceuticals is recalling Oxacillin for Injection (1 gram vials, Lot OXG301) due to lack of assured sterility. Approximately 65,710 vials distributed nationwide are affected.

    Product
    Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India. NDC 25021-146-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2231-2023·2023-08-02

    Flexiva Pulse ID Laser Fiber Recalled for Incorrect Component

    Boston Scientific is recalling Flexiva Pulse ID laser fibers due to an incorrect component that reduces power output and aiming beam brightness. The component can overheat, risking burns to users who touch the fiber connector.

    Product
    Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy Single-pack UPN: M006L8406910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2245-2023·2023-08-02

    Respiratory Diagnostic Test Kits Recalled for Decreased Performance Reliability

    Qiagen's QIAstat-Dx Respiratory SARS-CoV-2 Panel diagnostic kits are recalled due to decreased performance reliability. Failed test runs could require sample retesting, potentially delaying diagnosis.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended for analyzing nasopharyngeal swab (NPS) samples from patients suspected of respiratory infection for the presence of viral or bacterial nucleic acids REF 691223
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-2243-2023·2023-08-02

    Ventral Hernia Mesh Balloon May Fail to Inflate During Surgery

    A surgical mesh implant used in ventral hernia repair may fail to inflate properly during the procedure, potentially causing inadequate placement and infection risk. The manufacturer is recalling 169 units worldwide.

    Product
    Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450G (EU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0942-2023·2023-08-02

    Safe Tussin DM Cough Suppressant Recalled for Manufacturing Deviation

    Kramer Laboratories is recalling Safe Tussin DM Cough + Chest Congestion due to a manufacturing deviation involving non-food grade lubricant in the mixing vessel. Affected lots 8753, 8753A, and 8659 were distributed nationwide.

    Product
    Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2225-2023·2023-08-02

    Diagnostic Verification Product May Not Meet Shelf Life Stability Specifications

    Ortho-Clinical Diagnostics is recalling VITROS NT-proBNP II Range Verifiers Lot 0090 because the product may not meet shelf life stability specifications. Used for diagnostic system calibration verification.

    Product
    VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro diagnostic use only. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2246-2023·2023-08-02

    COVID-19 Diagnostic Test Kits Recalled Due to Performance Reliability Issues

    Qiagen has recalled 4155 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to decreased performance reliability. Test failures (run abortions) may require samples to be retested, potentially delaying diagnosis.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel (V1 and V2, CE IVD, not US IVD, not sold in the US.) Qualitative test intended for analyzing nasopharyngeal swab (NPS) samples from patients suspected of respiratory infection REF: 691214
    Category
    Medical Device
    Distribution
    14 states
  • SevereNHTSA·23V537000·2023-08-01

    Freightliner M2 Recalled for Driveshaft Breakage Risk

    Daimler Trucks North America is recalling 2023 Freightliner M2 vehicles because driveshafts can break under certain loading conditions, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E059000·2023-08-01

    SmartPlug Recalls 30A Shore Power Inlets Due to Fire Risk

    SmartPlug Systems is recalling 30A Shore Power Inlets because D-rings may crack, causing electrical arcing and fire.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V535000·2023-07-31

    Autocar Recalls 2023 Xpeditor Vehicles Due to Fuel Hose Defect

    Autocar is recalling 54 model-year 2023 Xpeditor vehicles because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V532000·2023-07-31

    Tiffin Recalls 2023 Phaeton Motorhomes Due to Fuel Hose Defect

    Tiffin is recalling 2023 Phaeton motorhomes because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V534000·2023-07-31

    2017-2022 Kia Niro vehicles recalled for engine compartment fire risk

    Kia is recalling 2017–2022 Niro and Niro Plug-in Hybrid vehicles because fluid may leak into the hydraulic clutch actuator, causing an engine compartment fire.

    Product
    KIA — KIA NIRO PHEV, NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V531000·2023-07-31

    2023 Kia Sportage vehicles recalled for electric oil pump fire risk

    Kia America is recalling certain 2023 Sportage vehicles due to a defective electric oil pump controller that may overheat and cause a vehicle fire. Dealers will inspect and replace the controller free of charge.

    Product
    KIA — KIA SPORTAGE, SELTOS, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V536000·2023-07-31

    Rosenbauer Fire Trucks Recalled for Winch Remote Water Ingress Risk

    Rosenbauer America is recalling specific fire trucks because water can enter the winch remote, causing corrosion that may allow the winch to operate unintentionally.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL M2-112, COMMERCIAL F-550, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V533000·2023-07-31

    Farber Specialty Ford Transit Recall for Fuel Hose Leak Risk

    Farber Specialty Vehicles is recalling one 2021 Ford Transit van because a fuel hose may leak gasoline, increasing the risk of fire.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V528000·2023-07-28

    Midway Specialty Vehicles Recalls 2022 Ford Transit Vans Due to Fuel Leak Risk

    Midway Specialty Vehicles is recalling 2022 Ford Transit vans with Cummins Onan generators because a fuel hose may leak gasoline, increasing fire risk.

    Product
    MIDWAY SPECIALTY VEHICLES — MIDWAY SPECIALTY VEHICLES FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V517000·2023-07-27

    Summit Bodyworks Recalls Ford Transit 350 Vehicles Due to Fuel Hose Defect

    Summit Bodyworks is recalling 2019-2022 Ford Transit 350 vehicles with specific generator sets because a fuel hose may not be secured, posing a fire risk.

    Product
    SUMMIT BODYWORKS — SUMMIT BODYWORKS FORD TRANSIT 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V516000·2023-07-27

    GM Recalls 2013 Vehicles for Driver Air Bag Inflator Defect

    General Motors is recalling 2013 Buick Verano, Chevrolet Camaro, Sonic, and Volt vehicles because the driver-side air bag inflator may explode during deployment.

    Product
    CHEVROLET — CHEVROLET, BUICK CAMARO, SONIC, VERANO, VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2023·2023-07-27

    Kingsland Recalls Frozen Meat and Poultry Produced Without Inspection

    Kingsland Food Processing Corp. is recalling various frozen meat and poultry products produced without federal inspection. No adverse reactions have been reported.

    Product
    Kingsland Food Processing Corp. Recalls Various Frozen Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide