The Recall Desk

State

Washington product recalls

20,188 recalls have nationwide distribution and so reach Washington. 0 additional recalls listed Washington specifically in their distribution scope.

About recalls in Washington

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Washington consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6926–6950 of 20188

  • HighFDA (Food)·F-0156-2025·2024-12-04

    Treehouse Foods Griddle Pancakes Recalled for Potential Listeria Contamination

    SE Grocers and Pics by Price Chopper brand griddle pancakes are being recalled by Treehouse Foods due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.

    Product
    SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR UPC 038259117194 PICS BY PRICE CHOPPER 12/16.5oz GRDL PNCK HSTYLE-PRCHP UPC 041735157386
    Category
    Food
    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 (Food)·F-0168-2025·2024-12-04

    Good & Gather and Breakfast Best Griddle Waffles Recalled for Listeria Risk

    Treehouse Foods is recalling Good & Gather and Breakfast Best griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected batches have codes starting with 2C with best-by dates between October 1, 2024 and October 11, 2025.

    Product
    GOOD & GATHER 12/12.3oz GRDL WFL BLBRY-GDGTR UPC 085239157923 BREAKFAST BEST 12/12.3 OZ GRDL WFL BLBRY-BKBST UPC 4061464782273
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0175-2025·2024-12-04

    Kodiak Cakes Buttermilk Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Kodiak Cakes griddle waffles (UPC 705599014802) due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the United States and Canada.

    Product
    KODIAK CAKES 8/14.8oz GRDL WFL BLGN BTRMLK VAN-KDKCS UPC 705599014802
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0063-2025·2024-12-04

    Drug recall: Absorbine Jr. Ultra Strength Pain Patch manufacturing deviations

    Absorbine Jr. Ultra Strength Pain Patch is being recalled nationwide due to manufacturing process deviations. The voluntary recall affects approximately 4,968,000 patches.

    Product
    ABSORBINE jr ULTRA STRENGTH PAIN PATCH, Menthol 6.5%, 1 patch per box, Distributed By: Absorbine Jr. LLC, Chattanooga, TN 37402 UPC 8 89476 41318 3, UPC 8 89476 41336 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V267000·2024-12-04

    Ford Bronco Sport Control Module Failure May Disable Drive Power

    Ford is recalling Bronco Sport and Maverick models due to control module defects that may fail to detect low battery charge, potentially disabling drive power and increasing crash risk. Dealers will provide free recalibration.

    Product
    FORD — 2022 FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0162-2025·2024-12-04

    H-E-B and Central Market Griddle Waffles Recalled for Listeria Risk

    H-E-B and Central Market brand griddle waffles with apple cinnamon are being recalled nationwide due to potential Listeria monocytogenes contamination affecting 9,907,389 cases.

    Product
    H-E-B 12/9oz GRDL WFL APL CIN ORG-HEBUT UPC 041220708376 CENTRAL MARKET 12/9oz GRDL WFL APL CIN ORG - CTMKT UPC 041220655748
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2025·2024-12-04

    Breakfast Best Griddle Pancakes Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Breakfast Best griddle pancakes nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates between October 1, 2024 and October 11, 2025.

    Product
    BREAKFAST BEST 8/33oz GRDL PNCK BDAY-BKBST UPC 4061459959116
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0213-2025·2024-12-04

    SELECTION Griddle Waffles Recalled Due to Potential Listeria Contamination

    Treehouse Foods is recalling SELECTION brand griddle waffles nationwide due to potential Listeria monocytogenes contamination. The recall affects about 9.9 million cases distributed in the USA and Canada.

    Product
    SELECTION 12/320g GRDL WFL WW-SLCTN UPC 059749977678
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0155-2025·2024-12-04

    Pancake and Griddle Mix Recalled for Potential Listeria Contamination

    Multiple brands of griddle pancake and buttermilk mix made by Treehouse Foods are being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.

    Product
    GIANT EAGLE 8/33oz GRDL PNCK BTRMLK - GT/EG UPC 030034071332 SCHNUCKS 8/33oz GRDL PNCK BTRMLK - SCHNK UPC 041318100020 SE GROCERS 8/33oz GRDL PNCK BTRMLK - SEGGR UPC 038259117170 BROOKSHIRE'S 8/33oz GRDL PNCK BTRMLK - BRKSH UPC 092825096740 SIGNATURE SELECT 8/33oz GRDL PNCK BTRML
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0192-2025·2024-12-04

    Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Kodiak Cakes griddle waffles due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C with best by dates from October 1, 2024 to October 11, 2025.

    Product
    KODIAK CAKES 8/10.72oz GRDL WFL DRKCH REFORM-KDKCS UPC 705599012709
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0072-2025·2024-12-04

    Parche Leon pain relief patches recalled for manufacturing deviations

    Unexo Life Sciences Private Limited is voluntarily recalling Parche Leon pain relief patches due to manufacturing practice deviations. No illnesses or injuries have been reported.

    Product
    PARCHE LEON — PARCHE LEON (CAPSAICIN, CAMPHOR, MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0554-2025·2024-12-04

    Shimadzu Autosampler Devices Subject to Water Damage Affecting Main Board

    Water condensation may accumulate under the autosampler's thermal insulation and damage the main board, causing communication errors and delays in laboratory testing. Two Shimadzu models are affected: SIL-40C XR CL and SIL-40C X3 CL.

    Product
    Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0064-2025·2024-12-04

    Absorbine Jr Pain Relieving Knee Patch recalled for manufacturing deviations

    Unexo Life Sciences is recalling Absorbine Jr Pain Relieving Knee Patch nationwide due to manufacturing process deviations that do not meet FDA standards. No illnesses or injuries have been reported.

    Product
    ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7%, packaged in a) 1 patch (UPC 8 89476 41251 3) and b) 6 patches (UPC 8 89476 41306 0), Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0070-2025·2024-12-04

    JR Watkins Menthol Pain Relief Patches Recalled for Manufacturing Deviations

    JR Watkins Cooling Pain Relief Patches are being recalled due to manufacturing process deviations identified during production.

    Product
    JR WATKINS COOLING PAIN RELIEF PATCHES, Menthol 7.5%, 5 patches per box, Distributed By: J.R. Watkins, LLC, Oakland, CA 94612 UPC 8 56294 00878 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0558-2025·2024-12-04

    Medline Endo Kit Recall: Missing Lot and Expiration Date Labels

    Medline is recalling Endo Kit models containing Olympus components with missing sterile and manufacturing lot numbers and expiration dates on packaging. Without this labeling, medical facilities cannot verify product expiration or track inventory.

    Product
    ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555
    Category
    Medical Device
    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
  • ModerateFDA (Drugs)·D-0071-2025·2024-12-04

    FDA Recalls Cheeky Bonsai Menthol Pain Relief Patches for Manufacturing Deviations

    Cheeky Bonsai Pain Relief Patches (Menthol 10%) are being recalled nationwide due to manufacturing facility compliance deviations. The voluntary recall affects 17,928 patches distributed across the US.

    Product
    CHEEKY BONSAI PAIN RELIEF PATCHES, Menthol 10%, 4 patches per box, Distributed by Cheeky Bonsai, San Francisco, CA UPC 8 60006 57564 9
    Category
    Drug
    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-0552-2025·2024-12-04

    Heart Device Transmitter Fails to Update Software After Power Interruption

    Abbott Medical's Merlin@home transmitter cannot upgrade to current software after power interruptions during prior downloads. This affects remote heart device monitoring systems.

    Product
    Merlin@home with the MerlinOnDemand capability Transmitter REF EX1150 Merlin@home with the MerlinOnDemand" (MoD) capability is a transmitter configured for multiple patient use. It can receive information from an implantable heart device in unpaired mode. With MoD capability
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0062-2025·2024-12-04

    Topical menthol back patch recalled for manufacturing deviations

    ABSORBINE jr. Extra Large Back Patch containing 5% menthol is being recalled nationwide due to manufacturing compliance deviations. The Class II recall affects 6,848,820 patches distributed by Absorbine Jr., LLC.

    Product
    ABSORBINE jr. Extra Large BACK PATCH, Menthol 5%, 1 extra large patch per box, Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402 UPC 8 89476 41218 6, UPC 8 89476 41236 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2025·2024-12-04

    LILAS Feminine Pain Relief Patch recalled for manufacturing violations

    Unexo Life Sciences is voluntarily recalling LILAS Feminine Pain Relief Patch nationwide due to manufacturing practice deviations affecting 363,300 patches.

    Product
    LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box (UPC 7 87099 48212 1) and 10 patches per box (UPC 7 87099 48211 4), Distributed by: Lilas Wellness, Inc., Beaverton, Oregon 97008-7105
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0520-2025·2024-12-04

    GE SIGNA and DISCOVERY PET/MR Scanners Recalled for Elevated Acoustic Noise

    GE Medical Systems is recalling SIGNA PET/MR and DISCOVERY PET/MR imaging systems because gradient coils can produce elevated acoustic noise during scanning under specific conditions.

    Product
    Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0068-2025·2024-12-04

    Equate Maximum Strength Lidocaine Pain Relieving Patches Recalled for Manufacturing Deviations

    Equate Maximum Strength Lidocaine Pain Relieving Patches (4%) are being recalled due to current Good Manufacturing Practice deviations. Approximately 1.1 million patches were distributed nationwide in the US.

    Product
    EQUATE PAIN RELIEVING PATCHES — EQUATE PAIN RELIEVING PATCHES (LIDOCAINE 4%)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0550-2025·2024-12-04

    GE Proteus XR/A radiographic system Wall Stand cable maintenance recall

    GE Healthcare is recalling certain Proteus XR/A radiographic systems because steel cables in the Wall Stand component have not been replaced at manufacturer-specified maintenance intervals.

    Product
    GE Proteus XR/A radiographic system
    Category
    Medical Device
    Distribution
    Distributed nationwide