The Recall Desk

State

Delaware product recalls

73,495 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.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24176–24200 of 76933

  • HighFDA (Devices)·Z-0189-2022·2021-11-10

    Arietta 750 Ultrasound Software Versions Affected by Incorrect Measurement Display

    FujiFilm Healthcare is recalling Arietta 750 Ultrasound Software versions V1.0.0 through V2.1.3 due to measurement display errors in critical cardiology functions that could lead to incorrect clinical diagnoses. The instruction manual also contains an error.

    Product
    Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0192-2022·2021-11-10

    Arietta 65 Ultrasound Software: Calculation Error in EROA Diagnostic Measurements

    Arietta 65 Ultrasound systems with software versions 1.0 through 4.0.0 contain a calculation error that produces incorrect measurements of cardiac valve function during diagnostic assessments.

    Product
    Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0196-2022·2021-11-10

    ADVIA Centaur SARS-CoV-2 Antigen Assay Recalled for Insufficient Validation Data

    Siemens Healthcare Diagnostics is recalling 261 ADVIA Centaur SARS-CoV-2 Antigen Assay test kits distributed nationwide because the FDA determined that validation data submitted for emergency authorization was insufficient to confirm the assay's effectiveness.

    Product
    ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207866
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0188-2022·2021-11-10

    FDA Recalls 3M Red Dot ECG Monitoring Electrodes Due to Potential Carbon Stud Breakage

    3M Red Dot ECG monitoring electrodes (Catalog No. 2244) are being recalled due to potential breakage of the carbon stud from the eyelet. Approximately 2,081,000 units distributed nationwide and internationally are affected.

    Product
    3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6, SAP ID: 7100212989), packaged 10 electrodes per card, 5 cards per pouch, 20 pouches per shipper box, 1,000 electrodes total per shipper box. The 3M Red Dot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0095-2022·2021-11-10

    Pharmanex Kids Jungamals dietary supplement missing fish allergen label

    NSE Products, Inc. is recalling Pharmanex Kids Jungamals dietary supplement because the label does not disclose fish allergen present in the product's Vitamin E ingredient.

    Product
    Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0086-2022·2021-11-10

    Lupin Irbesartan Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan 75 mg tablets due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient. The recall affects 51,144 bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2022·2021-11-10

    Dental Implants Mislabeled as Smaller Size; Risk of Nerve Damage

    GM Helix Acqua Implant dental implants were mislabeled as a smaller size. If incorrectly installed in cases with low bone quality, they could damage the nerve or adjacent bone structures.

    Product
    GM Helix Acqua Implant 3.5x10, Article No. 140.944
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2022·2021-11-10

    Dental implant recalled due to size mismatch with labeling

    Implant Direct Sybron Manufacturing is recalling 83 dental implants from lot 166300 because the implants differ in size from what is labeled on the packaging. The implants were distributed across multiple US states and Japan.

    Product
    ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22013·2021-11-10

    ABUS MountZ Youth Helmets Recalled for Head Injury Risk

    ABUS is recalling about 790 MountZ youth helmets that do not meet U.S. safety standards for bicycle helmets. The helmets pose a risk of head injury and should be returned for a full refund.

    Product
    ABUS MountZ Youth Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2022·2021-11-10

    Dental implants recalled for size mismatch with package labeling

    Implant Direct is recalling 61 dental implants because the packaged implants are a different size than declared on the labeling. Patients who may have received these implants should contact their healthcare provider.

    Product
    ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2022·2021-11-10

    MEDRAD Twist & Go Syringe Recalled Due to Labeling Error

    Bayer Medical Care is recalling 6,950 units of MEDRAD Twist & Go Disposable Syringes due to labeling errors that could cause confusion about syringe compatibility with the MEDRAD Mark 7 Arterion Injection System.

    Product
    The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a syringe made from a clear polycarbonate material and is an accessory to the MEDRAD Mark 7 Arterion Injection System. It is designed to be loaded into the injector head of the injection system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0083-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/80 mg) because the product was manufactured using an excipient that failed to meet conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0090-2022·2021-11-10

    Starbucks Doubleshot Espresso canned coffee recall due to sealing defect

    PepsiCo is recalling Starbucks Doubleshot Espresso canned coffee products due to inadequate sealing that may lead to premature spoilage. The recall affects approximately 85,956 cases distributed nationwide.

    Product
    Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 FL OZ UPC 012000008801
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/20 mg) nationwide because the product was manufactured using an excipient that failed conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0084-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed conductivity specifications. The recall affects 11,590 bottles of 30-count and 3,585 bottles of 90-count packages distributed nationwide.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0202-2022·2021-11-10

    Aspiration Syringe Kit MVSK60 Inadvertently Shipped with OUS Labeling

    MicroVention's Aspiration Syringe Kit (REF: MVSK60) was labeled for international distribution but inadvertently shipped to U.S. customers. The affected lot (H2146461) was distributed to Alabama, Nevada, and New York.

    Product
    Aspiration Syringe Kit, REF: MVSK60
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling 696 bottles of Ezetimibe and Simvastatin Tablets (10 mg/40 mg) distributed nationwide due to failed excipient specifications and the presence of foreign tablets in bottles.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0088-2022·2021-11-10

    Irbesartan 300 mg tablets recalled for impurity in active ingredient

    Lupin Pharmaceuticals is recalling Irbesartan 300 mg tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects approximately 119,544 bottles distributed nationally.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0201-2022·2021-11-10

    Medtronic Neuromodulation Clinician Programmer Application Software Anomaly Recall

    Medtronic recalled the Clinician Programmer Application (CPA) model A610 due to a potential software anomaly. Affected versions 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 have been distributed worldwide. No illnesses or injuries have been reported.

    Product
    Clinician Programmer Application (CPA) model A610 Clinician Software Application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0081-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Excipient Specification Failure

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/10 mg tablets nationwide because the product was manufactured using an excipient that failed to meet conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0089-2022·2021-11-10

    Starbucks Doubleshot Espresso canned coffee recalled for sealing defect

    PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Cream canned coffee products because inadequate sealing may cause premature spoilage.

    Product
    Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ UPC 012000001772
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0091-2022·2021-11-10

    Starbucks Doubleshot Espresso Canned Coffee Recall for Sealing Defect

    PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Salted Caramel Cream canned coffee products due to inadequate sealing that may lead to premature spoilage.

    Product
    Starbucks Doubleshot Espresso, Espresso & Salted Caramel Cream, 6.5 FL OZ UPC 012000007293
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V868000·2021-11-09

    2021 Tesla Model X and Model S driver air bags may tear during deployment

    Tesla is recalling certain 2021 Model X and Model S vehicles because the driver's air bag cushion may tear during deployment, potentially failing to protect occupants in a crash. Tesla will replace the air bag free of charge.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V867000·2021-11-08

    Hazard Lights Disabled When Ignition Off in Autocar Xpeditor Vehicles

    Autocar is recalling 2019-2022 Xpeditor vehicles because the hazard lights will not function with the ignition turned off. This violates federal safety standards and could increase crash risk in hazard situations.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide