The Recall Desk

State

Delaware product recalls

73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23901–23925 of 76924

  • HighFDA (Food)·F-0251-2022·2021-12-08

    Dom. Creme Ck Bag 50# Recall Due to Metal Contamination

    Puratos Corporation is recalling Dom. Creme Ck Bag 50# (Batch Number 10584006) due to possible contamination with metal fragments. The product was distributed domestically and to select foreign locations.

    Product
    Dom. Creme Ck Bag 50#. Material # 10584006
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0324-2022·2021-12-08

    Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect

    Boston Scientific is recalling the Hurricane RX Dilation Balloon nationwide due to a pinhole defect causing loss of pressure or failure to maintain pressure during endoscopic procedures used to treat biliary strictures.

    Product
    HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545930
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0329-2022·2021-12-08

    GE Centricity Medical Imaging Software May Display Incomplete Patient Studies

    GE Healthcare recalled versions of Centricity Universal Viewer Zero Footprint Client software due to a potential defect that could display incomplete patient imaging studies. No injuries have been reported.

    Product
    GE Centricity Universal Viewer Zero Footprint Client
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V948000·2021-12-08

    Carson Fun Runner Trailers Recalled for Potential Gas Leak Risk

    Carson is recalling 2018-2020 Fun Runner FC20 trailers because an overtightened bolt may damage the stove's o-ring, causing a gas leak that increases fire risk.

    Product
    CARSON — CARSON FUN RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0275-2022·2021-12-08

    Herbal Doctor Angelicae Sinensis Recalled for Elevated Lead and Cadmium

    Murray International Trading Co., Inc. is recalling "Herbal Doctor" brand Angelicae Sinensis herb packages due to elevated levels of lead and cadmium contamination. The product has been distributed to consumers across the eastern and central United States.

    Product
    "Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz (340g) packaged in a clear plastic box
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-0263-2022·2021-12-08

    Teg Creme Cake Bags Recalled for Potential Metal Contamination

    Puratos Corporation is recalling Teg Creme Cake Bags (50 lb) because they may contain foreign metal material. The affected product was distributed to customers in multiple U.S. states and internationally.

    Product
    Teg Creme Cake Bag 50#. Material #4107664
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0319-2022·2021-12-08

    NUVASIVE PRECICE Limb Lengthening System: Updated Instructions Clarify Patient Selection

    NuVasive is updating instructions for the PRECICE limb lengthening implant system to clarify it is for patients 18 years or older weighing 50 lbs or more, with no more than two devices implanted at a time.

    Product
    NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description: CPA1-000 PA0382-001 End Cap CPA2-000 PA1051-000 PACKAGED END CAP, 8.5/ 10.7MM, +0MM CPA2-005 PA1051-005 PACKAGED END CAP, 8.5/ 10.7MM, +5MM CPA2-010…
    Category
    Medical Device
    Distribution
    47 states
  • ModerateFDA (Food)·F-0254-2022·2021-12-08

    Easy Satin Supreme Creme Cake Bag contaminated with metal

    Puratos Corporation is recalling Easy Satin Supreme Creme Cake Bag 50# due to potential metal contamination. The affected product was distributed to bakery and food manufacturers in twelve U.S. states and two Caribbean countries.

    Product
    Easy Satin Supreme Creme Cake Bag 50#. Material #4107808
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0310-2022·2021-12-08

    Total Thyroxine ELISA Test Kits Recalled for Failed Quality Controls

    DRG International is recalling Total Thyroxine (T4) ELISA test kits due to failed quality controls affecting 314 units across multiple countries. The defective controls may delay diagnosis and waste patient samples.

    Product
    Total Thyroxine (T4) ELISA; REF EIA-1781
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-0235-2022·2021-12-08

    Tastykake Chocolate Creme Filled Cupcakes Recalled for Metal Fragments

    Flowers Foods is recalling Tastykake Chocolate Creme Filled Cupcakes due to the potential presence of small metal fragments in an ingredient. The affected product has an "Enjoy By" date of December 14 or December 18.

    Product
    Tastykake Chocolate Creme Filled Cupcakes 14.25oz, UPC 0 25600 00223 0
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·F-0249-2022·2021-12-08

    Puratos TK019 Chocolate Powder Blend Recalled for Metal Contamination

    Puratos Corporation is recalling approximately 119,900 lbs of TK019 2017 Choc Cup Powder Blend due to potential metal contamination. Affected batch numbers are 0010636571 and 0010636577.

    Product
    TK019 2017 Choc Cup Powder Blend Bag 50#. Item number 4005543
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0248-2022·2021-12-08

    TK006 Van Krimpet Powder Blend recalled for metal contamination

    Puratos Corporation is recalling TK006 Van Krimpet Powder Blend (50 lb bags, item number 4107780) because the product may contain foreign metal material. The affected batches are 0010636568 and 1110644921.

    Product
    TK006 Van Krimpet Powder Blend 50#. Item number 4107780
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0265-2022·2021-12-08

    Teg Moist'r Yellow Layer Cake Mix Recalled for Metal Contamination

    Puratos Corporation is recalling Teg Moist'r Yellow Layer Cake Mix (50# bag, Batch Number 10737143) due to potential metal contamination. The product was distributed to customers across 12 U.S. states and 2 foreign countries.

    Product
    Teg Moist'r Yellow Layer Cake Bag 50# Material #4107439
    Category
    Food
    Distribution
    11 states
  • LowFDA (Devices)·Z-0316-2022·2021-12-08

    INBONE Total Ankle System Recalled Due to Package Labeling Mismatch

    Wright Medical Technology is recalling the INBONE Total Ankle System because package contents do not match the package labeling on affected units distributed in Michigan and Pennsylvania.

    Product
    INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0264-2022·2021-12-08

    Tydemy Oral Contraceptive Recalled Due to Subpotent Drug

    Lupin Pharmaceuticals has recalled Tydemy oral contraceptive tablets nationwide due to subpotency. The recall affects 4,113 cartons distributed throughout the United States.

    Product
    Tydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets, 0.451 mg), packaged in cartons containing 3 wallets of 28 Tablets each, Rx Only, Distributed by: Lupin Pharmaceuticals, Inc., Baltimore, Maryland…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V943000·2021-12-07

    Great Dane Recalls 2022 Trailers Due to Wheel Hub Lubrication Defect

    Great Dane is recalling 2022 Champion and Everest trailers because insufficient wheel hub lubrication could cause bearing failure and loss of control.

    Product
    GREAT DANE — GREAT DANE CHAMPION, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22025·2021-12-06

    Drive DeVilbiss Adult Bed Rails Recalled; Two Deaths from Entrapment

    Drive DeVilbiss Healthcare is recalling four models of adult portable bed rails that can trap users between the rail and mattress, causing asphyxiation. Two deaths have been reported.

    Product
    Bed Assist Handles and Bed Assist Rail
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·046-2021·2021-12-05

    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Listeria

    Alexander & Hornung is recalling approximately 2.3 million pounds of fully cooked ham and pepperoni products due to possible Listeria monocytogenes contamination.

    Product
    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·045-2021·2021-12-03

    Erie Meat Products Recalls Chicken Bologna Imported Without Inspection

    Erie Meat Products Ltd. is recalling approximately 1,224 pounds of chicken bologna imported into the U.S. without FSIS reinspection. The products were distributed to correctional institutions in four states.

    Product
    Erie Meat Products Ltd. Recalls Chicken Bologna Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V940000·2021-12-03

    Zero Motorcycles Recalls 2022 SR Models Due to Incorrect Rear Brake Pads

    Zero Motorcycles is recalling 2022 SR, SR/F, and SR/S motorcycles because incorrect rear brake pads were installed, which may not work as intended and increase crash risk.

    Product
    ZERO — ZERO SR, SR/F, SR/S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V937000·2021-12-02

    2021 Hyundai Accent brake master cylinder defect recall

    Hyundai is recalling certain 2021 Accent vehicles due to a brake master cylinder defect. The component may have sharp edges that damage the inner oil seal, reducing braking performance and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V938000·2021-12-02

    2022 Hyundai Tucson: Inoperative Headlights and Taillights from Software Defect

    Hyundai is recalling 2022 Tucson vehicles with incompatible ICU software that can disable headlights and taillights, reducing visibility and increasing crash risk. All affected vehicles have been repaired.

    Product
    HYUNDAI — HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide