The Recall Desk

State

Delaware product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8851–8875 of 76427

  • HighFDA (Devices)·Z-0553-2025·2024-12-04

    Shimadzu Autosampler Water Intrusion May Cause Electrical Short Circuit

    Shimadzu laboratory autosamplers are being recalled due to water intrusion from a dehumidifier that can cause electrical short circuits. Affected units are distributed worldwide, including across the United States.

    Product
    Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2025·2024-12-04

    Philips SENSE Breast Coil Recall for Potential Patient Safety Hazard

    Philips is recalling 5,231 SENSE Breast Coils due to a potential patient safety hazard during scan preparation and performance. The FDA has not disclosed specific details about the nature of the risk.

    Product
    SENSE Breast Coil
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0515-2025·2024-12-04

    MEDLINE Epidural Procedure Kits: Connector May Prevent Catheter Insertion

    MEDLINE epidural trays used for labor anesthesia may have connectors that fail to fully open, preventing proper catheter insertion. The recall affects 2,592 units distributed across the US and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0511-2025·2024-12-04

    MEDLINE ultrasound procedure kit connectors recalled due to insertion malfunction

    Medline Industries is recalling procedure kits with connectors that may fail to open fully, preventing proper catheter insertion. The recall affects 3,396 units distributed in the U.S. and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0508-2025·2024-12-04

    Medline Nexus Catheter Connectors May Fail to Open Properly

    Medline recalls 1,975 NEXUS catheter connectors that may not fully open, preventing proper catheter insertion. Affected units were distributed nationwide and internationally.

    Product
    MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0546-2025·2024-12-04

    SENSE Breast Coil 3.0T recalled due to potential patient safety hazard

    Philips is recalling approximately 5,231 SENSE Breast Coil 3.0T units due to a potential safety hazard that could harm patients during MRI scanning procedures.

    Product
    SENSE Breast Coil 3.0T 7ch
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24E101000·2024-12-04

    Prestone Recalls DOT 3 Brake Fluid Bottles Containing Power Steering Fluid

    Prestone is recalling specific 1-gallon bottles of DOT 3 Brake Fluid that may contain power steering fluid. Using the wrong fluid can reduce braking performance and increase crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0204-2025·2024-12-04

    Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Kodiak Cakes griddle waffles nationwide due to potential Listeria monocytogenes contamination in batch codes starting with 2C.

    Product
    KODIAK CAKES 8/9.88oz GRDL WFL CINN MINI-KDKCS UPC 705599017162
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0152-2025·2024-12-04

    Treehouse Foods Recalls Frozen Waffles for Potential Listeria Contamination

    Treehouse Foods is recalling BREAKFAST BEST frozen griddle waffles nationwide due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases are affected; consumers should not eat the product.

    Product
    BREAKFAST BEST 12/12.3oz MXD CS GRDL WFL PMPKN/CINN-BKBST UPC 4061463257208
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0158-2025·2024-12-04

    KRUSTEAZ Griddle Pancake Mix Recalled Nationwide for Potential Listeria Contamination

    Treehouse Foods is recalling KRUSTEAZ Griddle Pancake Mix due to potential Listeria monocytogenes contamination. Approximately 9,907,389 cases with batch codes starting with '2C' and Best By dates from October 1, 2024, through October 11, 2025, are affected.

    Product
    KRUSTEAZ 12/15oz GRDL PNCK MINI BTRMLK-KTZCM UPC 686151200164
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0173-2025·2024-12-04

    Blueberry protein waffles recalled for potential Listeria contamination

    Multiple brands of frozen blueberry protein waffles are being recalled due to potential Listeria monocytogenes contamination. Products were distributed nationwide in the USA and Canada.

    Product
    H-E-B HIGHER HARVEST 12/10.72oz GRDL WFL BLBRY PRTN-HEBHH UPC 041220708093 BETTERGOODS 12/10.72oz GRDL WFL BLBRY PRTN-BTRGD UPC 194346252756 SIMPLE TRUTH 12/10.72oz GRDL WFL BLBRY PRTN - SMPTR UPC 011110108142 BREAKFAST BEST 12/13.4oz GRDL WFL BLBRY PRTN-BKBST UPC 4099100312997
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0176-2025·2024-12-04

    Wegmans griddle waffles recalled for potential Listeria contamination

    Treehouse Foods recalled 9,907,389 cases of Wegmans griddle waffles due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.

    Product
    WEGMANS 12/13.75oz GRDL WFL BLGN CIN - WEGMN UPC 077890550014
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0159-2025·2024-12-04

    Treehouse Foods Griddle Pancakes Recalled for Listeria Risk

    Treehouse Foods is recalling H-E-B and Trader Joe's griddle pancake products nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 through October 2025.

    Product
    H-E-B 12/14.1oz GRDL PNCK MINI HSTYLE ORG-HEBUT UPC 041220982714 TRADER JOE'S 16/11.3oz GRDL PNCK MINI HSTYLE ORG-TRDJO UPC 686151803778
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0188-2025·2024-12-04

    Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Kodiak Cakes griddle waffles due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the USA and Canada.

    Product
    KODIAK CAKES 8/14.8oz GRDL WFL BLGN CHOC CHIP-KDKCS UPC 705599015137
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0549-2025·2024-12-04

    Offset Cup Impactor Surgical Instruments Recalled for Weld Fracture

    INCIPIO DEVICES is recalling 100 units of Offset Cup Impactor surgical instruments (Lot 24A0087) because the TIG weld does not meet specifications and has fractured. These instruments are used in hip surgery to position acetabular cup implants.

    Product
    Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0215-2025·2024-12-04

    Grains of Paradise spice recalled for potential mold contamination

    Curio Spice Co. is recalling Grains of Paradise (Korerima) spice due to potential mold contamination. Affected consumers should discard the product.

    Product
    Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-0193-2025·2024-12-04

    Griddle Waffles with Flax Recalled Due to Listeria Contamination Risk

    Multiple brands of organic griddle waffles with flax are being recalled due to potential Listeria monocytogenes contamination. Affected products include Wegmans, H-E-B, Nature's Path Organic, and Central Market brands.

    Product
    WEGMANS 12/7.4oz GRDL WFL FLAX ORG - WEGMN UPC 077890481424 H-E-B 12/8.25oz GRDL WFL FLAX ORG-HEBUT UPC 041220708338 WEGMANS 12/8.25OZ 6CT GRDL WFL FLAX ORG-WEGMN UPC 077890577059 NATURES PATH ORGANIC 12/7.4oz GRDL WFL FLAX ORG - NPTHO UPC 058449590569 NATURES PATH ORGANIC 12/210
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0183-2025·2024-12-04

    Multiple Brands Griddle Waffles Recalled for Listeria Contamination Risk

    Multiple brands of griddle waffles manufactured by Treehouse Foods are being recalled nationwide due to potential Listeria monocytogenes contamination. Affected products include GOOD & GATHER, H-E-B HIGHER HARVEST, BETTERGOODS, BREAKFAST BEST, and SIMPLE TRUTH brands.

    Product
    GOOD & GATHER 12/10.72oz GRDL WFL BTRMLK VAN PRTN-GDGTR UPC 085239157961 H-E-B HIGHER HARVEST 12/10.72oz ORIG PRTN-HEBHH UPC 041220013685 BETTERGOODS 12/13.4oz GRDL WFL BTRMLK VAN PRTN-BTRGD UPC 194346252749 BREAKFAST BEST 12/13.4oz GRDL WFL BTRMLK VAN PRTN-BKBST UPC 409910031300
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0542-2025·2024-12-04

    Mammotrak Interventional Coil 1.5T recalled for patient safety risk

    Philips is recalling 5,231 units of the Mammotrak Interventional Coil 1.5T nationwide due to a potential safety issue that may harm patients during MRI preparation or scanning.

    Product
    Mammotrak Interventional Coil 1.5T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0535-2025·2024-12-04

    VITROS Chemistry CRP Diagnostic Slides May Underreport Elevated Results

    Ortho-Clinical Diagnostics is recalling 7,717 units of VITROS CRP diagnostic slides that may produce falsely low results for high C-reactive protein samples, risking missed diagnosis of infection or inflammation.

    Product
    VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/Catalog Number: 1926740
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2025·2024-12-04

    Philips ST SENSE Breast Imaging Coil Recalled for Patient Safety Risk

    Philips is recalling 5,231 units of the ST SENSE Breast Dx Coil nationwide due to a potential safety issue that may harm patients during breast imaging scans. No injuries have been reported.

    Product
    ST SENSE Breast Dx Coil
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2025·2024-12-04

    GE SIGNA Architect MRI Systems Recalled for Elevated Acoustic Noise

    GE Medical Systems is recalling certain SIGNA Architect MRI systems because their gradient coils can produce elevated acoustic noise during scanning under specific conditions, potentially risking hearing damage.

    Product
    SIGNA Architect, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0186-2025·2024-12-04

    Treehouse Foods recalls Nature's Path organic griddle waffles for Listeria contamination risk

    Treehouse Foods is recalling Nature's Path Organic griddle waffles due to potential Listeria monocytogenes contamination. The affected products were distributed nationwide in the United States and Canada.

    Product
    NATURES PATH ORGANIC 12/7.4oz GRDL WFL CHOC CHIP ORG GF-NPTHO UPC 058449167013 NATURES PATH ORGANIC 12/210g GRDL WFL CHOC CHIP ORG GF-NPOCN UPC 058449167006
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0066-2025·2024-12-04

    FDA Recalls Menthol Medicated Patches Due to Manufacturing Deviations

    FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.

    Product
    THERA CARE COLD HOT MEDICATED PATCH — THERA CARE COLD HOT MEDICATED PATCH (MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0551-2025·2024-12-04

    Abbott Merlin@home Cardiac Monitoring Transmitters Fail to Update After Power Loss

    Abbott is recalling 130 Merlin@home cardiac transmitters that cannot update software after power interruption during firmware download. Affected devices remain on outdated firmware with no ability to receive future updates.

    Product
    Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted heart device to Merlin.net" Patient Care Network (PCN) to facilitate remote monitoring by using inductive (EX1100 Model) or RF telemetry (E
    Category
    Medical Device
    Distribution
    Distributed nationwide