The Recall Desk

State

Washington product recalls

73,509 recalls have nationwide distribution and so reach Washington. 8,465 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,465
Critical
868
Severe
2,396
Most recent
2026-10-14

Of the 8,465 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.

These figures cover only the 8,465 recalls whose distribution notice names Washington specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24376–24400 of 81974

  • HighFDA (Drugs)·D-0372-2022·2022-01-19

    Nitroglycerin Lingual Spray Recalled for Defective Delivery System

    Padagis US LLC is recalling Nitroglycerin Lingual Spray due to a defective delivery system that may prevent proper medication administration. The recall affects 11,868 bottles distributed nationwide.

    Product
    NITROGLYCERIN LINGUAL — NITROGLYCERIN LINGUAL (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0485-2022·2022-01-19

    DePuy Joint Stem May Have Undersized Bore, Complicating Surgical Removal

    DePuy Orthopaedics has recalled 3 units of GLOBAL UNITE REV STEM SZ 8 due to an undersized spigot bore. Separation of the implant components may not be possible without surgical delay and/or bone damage.

    Product
    GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0362-2022·2022-01-19

    Metoprolol Tartrate Tablets Recalled for Foreign Metal in Tablets

    Rubicon Research Private Limited is recalling Metoprolol Tartrate 25 mg tablets (batch #210211H1, expiration February 2024) due to a complaint of metal embedded in a tablet.

    Product
    METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0486-2022·2022-01-19

    Hip stem implants recalled due to undersized bore defect

    DePuy Orthopaedics is recalling 781 hip stem implants that may have an undersized spigot bore diameter, potentially preventing surgical removal without additional surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0375-2022·2022-01-19

    Bosket Bread Brioche Dinner Rolls recalled for undeclared allergens

    Bosket Bread Company is recalling Brioche Dinner Rolls because the packages lack ingredient statements, leaving consumers unaware of potential allergen contents including wheat, milk, egg, soy, or sesame.

    Product
    Brioche Dinner Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0367-2022·2022-01-19

    Bosket Bread 8 Grain Bread recalled for undeclared allergens

    Bosket Bread Company is recalling 8 Grain Bread products sold in Washington because packages lack ingredient statements, leaving common allergens (wheat, milk, egg, soy, and sesame) undeclared.

    Product
    8 Grain Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0483-2022·2022-01-19

    Hip Stem Component Recalled Due to Undersized Bore Diameter

    DePuy is recalling GLOBAL UNITE STD STEM SZ 6 orthopedic stems due to undersized spigot bore that may prevent safe removal during revision surgery, risking surgical delays and bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0376-2022·2022-01-19

    Bosket Bread English Muffin Bread Recalled for Missing Ingredient Labels

    Bosket Bread Company is recalling English Muffin Bread products distributed in Washington because packages lack ingredient statements, leaving consumers unable to identify potential allergens including wheat, milk, egg, soy, or sesame.

    Product
    English Muffin Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0479-2022·2022-01-19

    Radiotherapy Planning Software BeamAdjust and VeriSoft Recalled for Measurement Errors

    PTW North America is recalling BeamAdjust 2.2 and VeriSoft 8.0 software due to measurement errors that can report incorrect radiation doses in patient treatment plans.

    Product
    Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0478-2022·2022-01-19

    OCT Camera Laser Safety Shut-Off Malfunction Affects Three Units

    Haag-Streit USA is recalling OCT-Camera 211 01 A3 units due to malfunction of the automatic laser beam shut-off. The device may not correctly recognize when the laser beam is safely switched off.

    Product
    OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0475-2022·2022-01-19

    CT Scanner Software Update Causes Head Image Quality Degradation

    Siemens SOMATOM Definition Edge CT scanners with software version VB20_SP5 may produce degraded head images, increasing the risk of patient misdiagnosis. Devices have been distributed nationwide.

    Product
    SOMATOM Definition Edge -Computed tomography system Model 10590000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0488-2022·2022-01-19

    Orthopaedic Stem Implants Recalled for Undersized Bore Manufacturing Defect

    DePuy Orthopaedics is recalling approximately 870 GLOBAL UNITE STD STEM implants worldwide because an undersized spigot bore may prevent proper separation, causing potential surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0473-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality

    Software version VB20_SP5 in certain Siemens CT scanners may degrade head image quality, increasing misdiagnosis risk. The recall affects 794 units distributed nationwide.

    Product
    SOMATOM Definition AS-Computed tomography system Model 8098027
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0399-2022·2022-01-19

    Raw Vegan Protein Peanut Butter Recalled for Undeclared Coconut

    NutraCap Labs LLC is recalling Raw Vegan Protein Peanut Butter dietary supplement because it contains undeclared coconut, which poses a risk to consumers with coconut allergies.

    Product
    RAW VEGAN PROTEIN PEANUT BUTTER NET WEIGHT 2.04LBS (925 GRAMS) DIETARY SUPPLEMENT Other Ingredients: Pea Protein Isolate, Brown Rice Protein, ***Sunflower (Non-Dairy) Creamer, Salt, Steviol Glycoside (95%) Manufactured in the U.S.A. for RAW, 838 SW Federal Highway, Stuart…
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0465-2022·2022-01-19

    Subdermal Needle Electrode Corkscrew Recall: Risk of Blue Hub Detachment

    Technomed Europe is recalling 117,672 disposable subdermal needle electrodes due to risk of the blue hub detaching, potentially leaving the needle in the patient's scalp.

    Product
    Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0378-2022·2022-01-19

    Bosket Bread Jalapeño Cheese Bread Recall: Undeclared Allergens

    Bosket Bread Company is recalling Jalapeño Cheese Bread sold in Washington because the packaging lacks an ingredient statement, leaving major allergens (wheat, milk, egg, soy, sesame) undeclared.

    Product
    Jalape¿o Cheese Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0371-2022·2022-01-19

    Bosket Bread Ciabatta Loaves Recalled for Undeclared Allergens

    Bosket Bread Company is recalling Ciabatta Loaves sold in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame undeclared. Consumers with allergies to these ingredients face a health risk.

    Product
    Ciabatta Loaves, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0487-2022·2022-01-19

    Orthopaedic Implant Stems Recalled for Undersized Spigot Bore Defect

    DePuy Orthopaedics is recalling GLOBAL UNITE REV STEM SZ 10 implants because the spigot bore may be undersized, preventing proper separation of components during revision surgery and potentially causing bone damage.

    Product
    GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2022·2022-01-19

    Bosket Bread Country Loaf recalled for undeclared allergens

    Bosket Bread Company is recalling Country Loaf bread products distributed in Washington because packages lack ingredient statements, creating risk of undeclared wheat, milk, egg, soy, or sesame exposure.

    Product
    Country Loaf, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0373-2022·2022-01-19

    Bosket Bread Cinnamon Rolls recalled for undeclared allergens

    Bosket Bread Company is recalling cinnamon rolls (1–1.5 lbs, packaged in plastic bags) distributed in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Cinnamon Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0368-2022·2022-01-19

    Bosket Bread Baguettes Recalled for Undeclared Allergens

    Bosket Bread Company is recalling baguettes distributed in Washington due to missing ingredient statements on packaging. The products may contain undeclared wheat, milk, egg, soy, or sesame.

    Product
    Baguettes, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Bread is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0469-2022·2022-01-19

    Sterilized medical convenience kits recalled for missing latex warning label

    ROi CPS LLC is recalling 195 Regard T AND A - Rogers sterilized convenience kits due to missing rubber latex warning labels. Consumers with latex allergies face risk of allergic reaction if exposed to the unlabeled latex.

    Product
    Regard, T AND A - Rogers, sterilized convenience kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0490-2022·2022-01-19

    Hip prosthetic stem undersized bore complicates removal surgery

    DePuy Orthopaedics' GLOBAL UNITE STD STEM prosthetics may have undersized spigot bores, complicating removal during revision surgery. Affected patients may experience surgical delays or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0489-2022·2022-01-19

    Hip Stem Device Recalled Due to Undersized Bore Diameter Risk

    DePuy Orthopaedics recalls the GLOBAL UNITE STD STEM SZ 14 hip stem in 451 units worldwide due to undersized spigot bore diameter. The defect may prevent proper separation of the stem during surgery without surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0470-2022·2022-01-19

    RefleXion Medical Radiotherapy System Recall Due to Dose Discrepancy

    Reflexion Medical is recalling three RefleXion X1 radiotherapy systems due to a potential dose discrepancy when delivering treatment in Feet First Supine patient orientation.

    Product
    RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: "RefleXion X1 Model: RXM1000"
    Category
    Medical Device
    Distribution
    Distributed nationwide