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.

4176–4200 of 76375

  • HighFDA (Devices)·Z-0584-2026·2025-12-03

    Blood lead test kits recalled over mislabeled calibration buttons

    Magellan Diagnostics is recalling 1,774 LeadCare II Blood Lead Test Kits because calibration buttons used in kitting were labelled with the wrong lot number.

    Product
    The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2026·2025-12-03

    Demonstration only gel recalled because it may be placed in patients

    Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.

    Product
    Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0601-2026·2025-12-03

    Brain access devices recalled because packaging tape contains latex

    Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2026·2025-12-03

    IV set 490487 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V836000·2025-12-03

    Volkswagen ID.4 recalled for high-voltage battery fire risk

    Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2026·2025-12-03

    Anesthesia vaporizers recalled over the potential for anesthesia leakage

    Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.

    Product
    Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0179-2026·2025-12-03

    Saline nasal spray recalled over microbial contamination with Pseudomonas lactis

    Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.

    Product
    Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V835000·2025-12-03

    2026 Volkswagen ID.4 and Atlas vehicles recalled for incorrect wheel bolts

    Volkswagen is recalling 27 vehicles with potentially incorrect wheel bolts that could detach during driving. Owners should not drive their vehicles until bolts are inspected and replaced by a dealer at no cost.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4, ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0594-2026·2025-12-03

    Diabetes clinic software recalled over incorrect sensor glucose graph data

    Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.

    Product
    CareLink Clinic, REF: MMT-7350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0589-2026·2025-12-03

    Vena cava filters recalled over resistance when advancing the dilator

    Argon Medical Devices is recalling 1,821 Option ELITE Vena Cava Filter Systems after complaints of increased resistance when advancing the dilator within the introducer sheath.

    Product
    Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2026·2025-12-03

    Heated massage tables recalled over heat components that can smolder

    Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0587-2026·2025-12-03

    Q400 massage tables recalled over heat components that can overheat

    Pivotal Health Solutions is recalling 34 Quantum Intersegmental Tables, model Q400, because damage to the heat function components can lead to overheating and smoldering.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0581-2026·2025-12-03

    Vitrectomy probe packs recalled with no reason stated in the record

    Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.

    Product
    CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+ B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0585-2026·2025-12-03

    Culture media recalled over contamination that may darken the broth

    Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.

    Product
    1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V834000·2025-12-02

    Zero Recalls 2023 DSR/X Motorcycles Due to Motor Controller Defect

    Zero Motorcycles is recalling 2023 DSR/X motorcycles because incorrect fasteners in the motor controller may cause a loss of drive power, increasing crash risk.

    Product
    ZERO — ZERO DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V827000·2025-12-01

    Ford Recalls 2016-2019 Lincoln MKT for Detaching B-Pillar Trim

    Ford is recalling 2016-2019 Lincoln MKT vehicles because the B-pillar door trim may detach while driving, creating a road hazard and increasing crash risk.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V824000·2025-12-01

    2019 Ram Trucks Recalled for Side Curtain Air Bag Inflator Defect

    Chrysler is recalling 2019 Ram 1500, 2500, and 3500 vehicles because side curtain air bag inflators may rupture, potentially sending metal fragments into the cabin.

    Product
    RAM — RAM 1500, 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V828000·2025-12-01

    Ford Recalls 2025 Maverick for Cylinder Head Manufacturing Defect

    Ford is recalling 2025 Maverick vehicles with defectively manufactured cylinder heads that can leak oil. The leak increases the risk of fire and engine failure.

    Product
    FORD — FORD, LINCOLN EXPLORER, MUSTANG, MAVERICK, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V832000·2025-12-01

    Virnig Recalls 2025 Trailers Due to Bearing Lock Nut Failure Risk

    Virnig is recalling 2025 TR-HDD-1414 and TR-RHDD-1409 trailers because improperly installed bearing lock nuts may fail, causing the tire to detach and increasing crash risk.

    Product
    VIRNIG — VIRNIG TR-RHDD-1409, TR-HDD-1414
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V831000·2025-12-01

    2025 Lincoln Navigator Rear Lightbar Cracks May Disable Reverse Lights

    Ford is recalling certain 2025 Lincoln Navigator vehicles. The rear lightbar may develop cracks allowing moisture accumulation, potentially disabling reverse lights and reducing visibility when backing up.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V829000·2025-12-01

    2025 Ford Escape liftgate hinge covers may detach, creating crash risk

    Ford is recalling certain 2025 Escape vehicles because liftgate hinge covers may not be properly secured and can detach. Detached covers can create a distraction or road hazard, increasing crash risk.

    Product
    FORD — FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V833000·2025-12-01

    Genesis G90 Models: Highway Drive Assist Braking Malfunction Recall

    Hyundai is recalling 2023-2026 Genesis G90 vehicles because the Highway Drive Assist radar may falsely detect another vehicle, causing sudden braking that increases crash risk.

    Product
    GENESIS — GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V826000·2025-12-01

    2025-2026 RAM Pickup Trucks: Blank Instrument Panel Display Software Error

    Chrysler is recalling 2025-2026 RAM pickup trucks (1500, 2500, 3500, 4500, 5500) because a software error causes the instrument panel display to go blank, preventing drivers from seeing critical warning lights and gear selection.

    Product
    RAM — RAM 1500, 2500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide