The Recall Desk

State

Washington product recalls

73,741 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,535
Critical
865
Severe
2,404
Most recent
2026-10-28

Of the 8,535 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 2,404 (28%) are Severe.

These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35401–35425 of 82276

  • SevereFDA (Drugs)·D-1863-2019·2019-09-25

    West-Ward Recalls Oxcarbazepine Oral Suspension Due to Impurity Failures

    West-Ward Columbus Inc is recalling specific lots of Oxcarbazepine Oral Suspension because they failed impurity and degradation specifications.

    Product
    Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, Distr. by: West-Ward Pharmaceuticals,Eatontown, NJ. NDC:0054-0199-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2199-2019·2019-09-25

    PitaPal Organic Cilantro Jalapeno Hummus Recalled for Listeria Risk

    Pita Pal Foods LP is recalling PitaPal Organic Cilantro Jalapeno Hummus due to potential Listeria monocytogenes contamination.

    Product
    PitaPal Organic Cilantro Jalapeno Hummus 10 oz. UPC 851570003348 packaged in Plastic tub with clear lid with green rim.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2541-2019·2019-09-25

    Wilson-Cook Recalls Hemospray Endoscopic Hemostat Due to Misassembly

    Wilson-Cook Medical Inc. is recalling 160 units of Hemospray Endoscopic Hemostat because misassembly may prevent the device from spraying powder.

    Product
    Hemospray Endoscopic Hemostat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V679000·2019-09-25

    Volkswagen Recalls Multiple Models Due to Regulatory Non-Compliance

    Volkswagen is recalling specific 2007-2019 models because internal evaluation modifications may cause non-compliance with regulatory requirements, potentially increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, PASSAT, JETTA HYBRID, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2544-2019·2019-09-25

    Ad-Tech Drill Sleeve Guides Recalled for Potential Drill Bit Seizure

    Ad-Tech Medical Instrument Corporation is recalling specific Drill Sleeve Guides because the inner diameter was under tolerance, which could cause the drill bit to seize during surgery.

    Product
    AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-2543-2019·2019-09-25

    Boston Scientific Recalls S-ICD Devices Due to Battery Depletion

    Boston Scientific is recalling 404 EMBLEM MRI S-ICD devices because a compromised electrical component causes accelerated battery depletion, potentially requiring earlier replacement.

    Product
    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2542-2019·2019-09-25

    Boston Scientific Recalls 28 Subcutaneous Implantable Cardioverter Defibrillators

    Boston Scientific is recalling 28 EMBLEM S-ICD devices due to accelerated battery depletion. Patients should contact their healthcare provider for evaluation.

    Product
    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2547-2019·2019-09-25

    Philips IntelliVue Remote Antenna Cable Recalled for Incorrect Rating

    Philips is recalling IntelliVue 1.4 GHz Remote Antenna cables used with MX40 monitors because they lack the required rating for some installations.

    Product
    IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded twisted pair data cable bundle and is a component of the Philips Remote Antenna (PN 867151). The Remote Antenna is used with IntelliVue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1862-2019·2019-09-25

    Torrent Pharma Recalls Anagrelide Capsules Due to Impurity Failures

    Torrent Pharma Inc. is recalling 2,472 bottles of Anagrelide Capsules because routine stability testing detected high levels of impurities.

    Product
    ANAGRELIDE — ANAGRELIDE (ANAGRELIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1870-2019·2019-09-25

    Aurolife Pharma Recalls Fexofenadine Hydrochloride Tablets for Impurity Failures

    Aurolife Pharma is recalling specific lots of 180 mg Fexofenadine Hydrochloride tablets because they failed impurity and degradation specifications.

    Product
    Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 62011-0315-1); and b) 30-count cartons (NDC 62011-0315-2) HealthMart PHARMACY, Distributed by McKesson, One Post Street, San Francisco, CA 94104.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1865-2019·2019-09-25

    Aurolife Pharma Recalls Allergy Relief Tablets Due to Impurity Failures

    Aurolife Pharma is recalling specific lots of Allergy Relief (Fexofenadine Hydrochloride) 180 mg tablets because they failed impurities and degradation specifications.

    Product
    Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b) 30-count cartons (NDC 60000-409-30); c) 45-count bonus cartons (NDC 60000-409-48); d) 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2545-2019·2019-09-25

    CooperSurgical Recalls LEEP Return Patient Pads Due to Expiration Date Errors

    CooperSurgical is recalling LEEP Return Patient Pads because the expiration dates on the outer boxes have the month and day reversed compared to the individual pouches.

    Product
    LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V676000·2019-09-23

    Mercedes-Benz Recalls E-Class Wagons Due to Rear Spoiler Detachment Risk

    Mercedes-Benz is recalling specific 2017-2019 E-Class wagons because the rear spoiler may detach while driving, creating a road hazard and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, E63S, E 400, E400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V674000·2019-09-23

    Spartan Metrostar and Gladiator Recall for Air Brake Control Line Defect

    Spartan is recalling 2004-2020 Metrostar and Gladiator vehicles because unprotected air brake control lines may cause unexpected brake application and increase crash risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V673000·2019-09-23

    Pleasure Way Recalls 2018-2020 Motorhomes for Awning Drive Mechanism Failure

    Pleasure Way is recalling 2018-2020 Plateau, Ascent, and Lexor motorhomes because the awning drive mechanism may fail, causing the awning to extend unexpectedly.

    Product
    PLEASURE WAY — PLEASURE WAY ASCENT, PLATEAU, LEXOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V668000·2019-09-20

    Forest River Recalls 2020 Cherokee Trailers Due to Wiring Exposure

    Forest River is recalling 2020 Cherokee trailers because missing protective paneling exposes distribution panel wiring, increasing the risk of electrical shock or fire.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V675000·2019-09-20

    Ducati Recalls 2014-2018 Motorcycles Due to Engine Oil Leak Risk

    Ducati is recalling 651 motorcycles because engine oil may leak into the airbox and drip onto the rear tire, increasing crash risk.

    Product
    DUCATI — DUCATI 1199, 1299, PANIGALE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·093-2019·2019-09-20

    Frozen Chicken Entrees Recalled for Misbranding and Undeclared Soy Allergen

    Astrochef LLC is recalling frozen chicken entrees labeled as beef due to misbranding and undeclared soy. No adverse reactions have been reported.

    Product
    Pegasus Foods Inc. — Astrochef LLC. Recalls Chicken Pub Style Entrees Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    10 states
  • SevereNHTSA·19V667000·2019-09-19

    GM Recalls 2019-2020 Chevrolet Equinox AWD for Fuel Tank Leak Risk

    General Motors is recalling 2019-2020 Chevrolet Equinox all-wheel drive vehicles because improperly sealed fuel tank seams may leak fuel, increasing fire risk.

    Product
    CHEVROLET — CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide