The Recall Desk

State

Washington product recalls

73,817 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,536
Critical
865
Severe
2,405
Most recent
2026-11-04

Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45876–45900 of 82353

  • SevereFDA (Drugs)·D-1121-2017·2017-08-30

    Major Senna Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1120-2017·2017-08-30

    Rugby Diocto Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1122-2017·2017-08-30

    Rugby Aller-chlor Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1123-2017·2017-08-30

    Rugby Senexon Liquid Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3054-2017·2017-08-30

    Medtronic AxiEM ENT Suction Devices Recalled for Verification Failure

    Medtronic is recalling 60 reusable ENT suction instruments because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.

    Product
    Medtronic Suction 9734308 Small AxiEM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3059-2017·2017-08-30

    Custom Assemblies Recalls Custom Surgical Kits with Defective BD Needles

    Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.

    Product
    Various custom surgical kits manufactured for CMS, CUSTOM MEDICAL SPECIALTIES, INC.: (a) CMS-4153-R2 MPM Biopsy TRAY (b) CMS-5832-R1 Custom Safety Mammo Biopsy Tray (c) CMS-4108 Multipurpose Safety Tray (d) CMS-3141-R6 Custom Ultrasound Tray (e) CMS-2891-R1 Custom Safety…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3428-2017·2017-08-30

    Mary's Harvest Recalls Tandoori Grain Salad Due to E. coli Risk

    Mary's Harvest Fresh Foods is recalling Tandoori Grain & Vegetable Salad due to potential E. coli O26 contamination.

    Product
    Kroger QFC, Tandoori Grain & Vegetable Salad, net wt. 10 oz, UPC 8 267661445 3.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·17V538000·2017-08-30

    REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Wiring Defect

    REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER JAMBOREE, VESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3066-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans SFILL 360 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans SFILL 360, 3-TT-SFILL 360. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3049-2017·2017-08-30

    Alcon ORA System Recall for Incorrect IOL Power Measurements

    Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.

    Product
    ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3061-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 250 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3052-2017·2017-08-30

    Medtronic Curved Suction 70 Recalled for Verification Failure

    Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.

    Product
    Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3063-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 1000 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3064-2017·2017-08-30

    FDA Recalls Tissu-Trans Filtron 2000 Due to Sterile Seal Integrity Concerns

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.

    Product
    Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3416-2017·2017-08-30

    Mary's Harvest Broccoli Products Recalled for Potential E. coli O26 Contamination

    Mary's Harvest Fresh Foods is recalling specific broccoli products due to potential contamination with E. coli O26. The products were distributed in Oregon and Washington.

    Product
    Kroger (QFC and Fred Meyer) brand, Broccoli Floret KFK, Net wt. 8 oz , UPC 8 2676618506 1. Kroger Main & Vine brand, Broccoli Floret, Net wt. 8 oz, UPC 8 2676618750 8. Mary's Harvest brand, Broccoli Buds or Broccoli Florette, Net wt. 16 oz, UPC 8 8724180456 3. Mary's…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-3065-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3427-2017·2017-08-30

    Mary's Harvest Stir Fry Vegetables Recalled for E. coli O26 Risk

    Mary's Harvest Fresh Foods is recalling 5 lb. packages of Stir Fry Vegetables due to potential contamination with E. coli O26. The product was distributed in Oregon and Washington.

    Product
    Mary's Harvest, STIR FRY VEGETABLES STORE PACK, net wt. 5 lb. No UPC. Ingredients statements: Broccoli, Green peppers, Carrot, Red Peppers, Yellow Onion, Red Onion, Yellow Peppers, Snow Peas, Daikon Radish.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3408-2017·2017-08-30

    New Seasons Market Recalls Rainbow Carrot and Quinoa Salad for Undeclared Allergens

    New Seasons Market is recalling Rainbow Carrot and Quinoa Salad because it contains undeclared wheat and pecans. The product was sold in Oregon and Washington.

    Product
    Rainbow Carrot and Quinoa Salad, ready to eat product, packaged in one pint clear plastic deli containers, sold at random weight. UPC 252383-001604.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-3058-2017·2017-08-30

    Medtronic ENT Navigation Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.

    Product
    Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). The firm name on the label is Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3419-2017·2017-08-30

    Mary's Harvest Broccoli Kit Recalled for Potential E. coli O26 Contamination

    Mary's Harvest Fresh Foods is recalling SLD Broccoli Kits due to potential E. coli O26 contamination. The product was distributed in Oregon and Washington.

    Product
    Mary's Harvest brand, SLD BROCCOLI KIT, net wt. 6 lb. No UPC. Ingredients statement: Broccoli, Broccoli Slaw Blend, Coleslaw dressing, Red Onion, Raisin, Sun Flower seeds, Bacon Bits. Contains Egg
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3421-2017·2017-08-30

    Mary's Harvest Vegetable Trays Recalled for Potential E. coli O26 Contamination

    Mary's Harvest Fresh Foods, Inc. is recalling specific Vegetable Tray Rectangle packages due to potential contamination with E. coli O26.

    Product
    Mary's Harvest brand, Vegetable Tray Rectangle, 4/40 oz. packages, UPC 0 9250475701 6. Mary's Harvest brand, Vegetable Tray Rectangle, 4/18 oz packages, UPC 0 9250475712 2. Ingredients: Celery, Grape Tomatoes, Sugar Snap Peas, Broccoli, Carrots, and Ranch Dip.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3418-2017·2017-08-30

    Mary's Harvest Vegetable Medley Recalled for Potential E. coli O26 Contamination

    Mary's Harvest Fresh Foods is recalling specific vegetable medley products due to potential contamination with E. coli O26.

    Product
    Kroger (QFC and Fred Meyer) brand, VEGETABLE MEDLEY KFK, Net wt. 10 oz, UPC 8 2676618505 4. Kroger Main & Vine brand, VEGETABLE MEDLEY, Net wt. 10 oz, UPC 8 2676618749 2. Mary's Harvest brand, Rainbow Veggies, 6/24 oz. packages, UPC 0 9250438263 8. Mary's Harvest…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3432-2017·2017-08-30

    Mary's Harvest Veggie Cup Recalled for Potential E. coli O26 Contamination

    Mary's Harvest Fresh Foods, Inc. is recalling specific Veggie Cup packages due to potential contamination with E. coli O26. The product was distributed in Oregon and Washington.

    Product
    Mary's Harvest, Veggie Cup, 6/12 oz pacakges, UPC 0 9250470153 8. Marys Harvest, Veggie Cup, 6/ 8 oz packages, UPC 0 9250470021 0.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3423-2017·2017-08-30

    Mary's Harvest Stir Fry Asian Recalled for E. coli O26 Contamination

    Mary's Harvest Fresh Foods is recalling Stir Fry Asian packages due to potential E. coli O26 contamination. The product was distributed in Oregon and Washington.

    Product
    Mary's Harvest brand, Stir Fry Asian, 6/18 oz packages, UPC 8 8724179812 1. Ingredients statements: Green Pepper, Broccoli, Red Pepper, Snow Peas, White Onion, Red Onion, Bok Choy, Carrot, Mushrooms, Baby Corn, Bamboo Shoots, and Water Chestnuts.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·17V539000·2017-08-30

    New Flyer Transit Bus Seat Belt Buckle Recall

    New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.

    Product
    NEW FLYER — NEW FLYER MD30, XD40, XN40, MD35
    Category
    Vehicle
    Distribution
    Distributed nationwide