The Recall Desk

State

Delaware product recalls

72,940 recalls have nationwide distribution and so reach Delaware. 3,435 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,435
Critical
477
Severe
937
Most recent
2026-09-09

Of the 3,435 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 937 (27%) are Severe.

These figures cover only the 3,435 recalls whose distribution notice names Delaware specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4451–4475 of 76375

  • HighFDA (Devices)·Z-0432-2026·2025-11-12

    Hip bipolar heads recalled over packaging that may compromise sterility

    Total Joint Orthopedics is recalling 103 Klassic BiPolar Heads over a potential packaging issue that could compromise the sterile barrier and present a risk of infection if implanted.

    Product
    Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic BiPolar Head, 41 mm OD, 22 mm Head; 3205.42.022 Klassic BiPolar Head, 42 mm OD, 22 mm Head; 3205.43.022 Klassic BiPolar Head, 43 mm OD, 22 mm Head; 3205.44.028 Klassic BiPolar Head, 44 mm OD, 28 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0423-2026·2025-11-12

    Curved extension catheter trays 20 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with curved extensions, 12 Fr x 20 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0163-2026·2025-11-12

    Easy peel deveined shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,800 cases of AquaStar 13/15 Raw Shrimp Easy Peel Deveined, sold at Publix, because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0439-2026·2025-11-12

    bk3500 ultrasound systems recalled over incomplete battery safety instructions

    B-K Medical is recalling 124 bk3500 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk3500 Ultrasound System w/battery; Model No. 2300-41; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0440-2026·2025-11-12

    Ultrasound systems recalled over battery guidance missing from the manuals

    B-K Medical is recalling 895 bk5000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk5000 Ultrasound System w/battery; Model No. 2300-61; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0438-2026·2025-11-12

    bk3000 ultrasound systems recalled over incomplete battery replacement guidance

    B-K Medical is recalling 496 bk3000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk3000 Ultrasound System w/battery; Model No. 2300-66; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0435-2026·2025-11-12

    Flex Focus ultrasound carts recalled over incomplete battery safety instructions

    B-K Medical is recalling 4,426 1202 Flex Focus ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0436-2026·2025-11-12

    bkSpecto ultrasound systems recalled over battery guidance gaps in manuals

    B-K Medical is recalling 1,697 Ultrasound System 1300 bkSpecto units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    Ultrasound System 1300, bkSpecto w/battery; Model No. 1300-21 or 1300-S1; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0437-2026·2025-11-12

    bkActiv ultrasound systems recalled over battery guidance missing from manuals

    B-K Medical is recalling 567 Ultrasound System 2300 bkActiv units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    UUltrasound System 2300, bkActiv w/battery; Model No. 2300-11; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V773000·2025-11-10

    Nova Bus Recalls 2024-2025 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2024-2025 LFS transit buses because the driver's seat belt may be pinched by the partition, preventing proper retraction and increasing injury risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E074000·2025-11-07

    AROW Emergency Exit Window Latch Failure Recall

    AROW Global Corp is recalling emergency exit windows because the latch can fail during a crash, increasing the risk of passenger injury.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V768000·2025-11-06

    GM Recalls 2019-2020 Chevrolet Silverado Medium Duty Trucks for Brake Wiring Defect

    General Motors is recalling 2019-2020 Chevrolet Silverado 4500, 5500, and 6500 trucks because a brake jumper wire harness may lack protective tape, risking power brake assist failure.

    Product
    CHEVROLET — CHEVROLET SILVERADO 6500, SILVERADO 5500, SILVERADO 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V766000·2025-11-06

    Jeep Grand Cherokee and Wrangler 4XE vehicles engine debris recall

    Chrysler is recalling certain 2023–2025 Jeep Grand Cherokee 4XE and 2024–2025 Jeep Wrangler 4XE vehicles due to debris inside the engine that may cause engine failure, loss of drive power, and engine compartment fire.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE, WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V765000·2025-11-06

    RAM pickup trucks steering column control module air bag risk

    Chrysler is recalling certain 2021–2022 RAM 1500, 2500, 3500, 4500, and 5500 vehicles because the steering column control module may prevent the driver's side air bag from deploying in a crash, increasing injury risk.

    Product
    RAM — RAM 3500, 2500, 4500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V769000·2025-11-06

    GMC Recalls 2026 Hummer EV Models Due to Air Bag Wiring Defect

    General Motors is recalling 2026 GMC Hummer EV Pickup and SUV vehicles because an improperly crimped wire may prevent the front passenger air bag from deploying.

    Product
    GMC — GMC HUMMER EV SUV, HUMMER EV PICKUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26068·2025-11-06

    Prosecco bottles recalled after ten reports of shattering and one laceration

    About 941,400 bottles of Kirkland Signature Valdobbiadene Prosecco DOCG are being recalled because the bottles can break or shatter; ten reports include one laceration injury.

    Product
    Kirkland Signature Valdobbiadene Prosecco DOCG bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V764000·2025-11-06

    GM Recalls 2014 Buick Verano and Chevrolet Cruze for Air Bag Defect

    General Motors is recalling 2,099 vehicles because side roof-rail air bag inflators may rupture, potentially causing sharp metal fragments to enter the vehicle.

    Product
    BUICK — BUICK, CHEVROLET VERANO, CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26067·2025-11-06

    Exercise bikes recalled after seat posts broke and riders fell

    About 833,000 Peloton Original Series Bike+ units are being recalled after three reports of the seat post breaking and detaching during use, including two fall injuries.

    Product
    Peloton Original Series Bike+ Model PL02
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26070·2025-11-06

    Children's scooters recalled after 18 reports of a front wheel detaching

    About 50 three-wheeled children's scooters are being recalled after 18 reports of the left front wheel detaching during use, resulting in three injuries.

    Product
    Three-Wheeled Children's Scooter with Foot Brake
    Category
    Consumer Product
    Distribution
    Distributed nationwide