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.

44251–44275 of 82353

  • CriticalFDA (Food)·F-0805-2018·2018-02-14

    Panera Plain Cream Cheese Recalled for Listeria Contamination Risk

    Panera, LLC is recalling Plain Cream Cheese in 2 oz. and 8 oz. sizes due to potential Listeria monocytogenes contamination. The product was sold nationwide at Panera Cafes.

    Product
    Panera Plain Cream Cheese, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0807-2018·2018-02-14

    Panera Cream Cheese Recalled Over Listeria Contamination Risk

    Panera is recalling Reduced-Fat Honey Walnut Cream Cheese due to potential Listeria monocytogenes contamination. The product was sold nationwide at Panera Cafes.

    Product
    Panera Reduced-Fat Honey Walnut Cream Cheese, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0808-2018·2018-02-14

    Panera Recalls Reduced-Fat Wild Blueberry Cream Cheese Due to Listeria Risk

    Panera, LLC is recalling Reduced-Fat Wild Blueberry Cream Cheese because it may be contaminated with Listeria monocytogenes. The product was sold nationwide at Panera Cafes.

    Product
    Reduced-Fat Wild Blueberry Cream Cheese, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0774-2018·2018-02-14

    Bulletproof Collagen Protein Recalled for Undeclared Milk Allergen

    Bulletproof 360 Inc is recalling Unflavored Collagen Protein because the product contains undeclared milk. The item is mislabeled as collagen protein but actually contains whey protein.

    Product
    Bulletproof Unflavored Collagen Protein High Performance Building Blocks Dietary Supplement, packaged in a 16-oz. composite-film bag, UPC: 8 15709 02115 3. The label is read in parts: "***COLLAGEN PROTEIN***Ingredients: Hydrolyzed collagen powder***Processed in a facility…
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Drugs)·D-0339-2018·2018-02-14

    Aurobindo Recalls Ampicillin and Sulbactam Injection Due to Glass Particulates

    Aurobindo Pharma is recalling 53,040 vials of Ampicillin and Sulbactam for Injection due to a confirmed report of visible glass particulate matter.

    Product
    AMPICILLIN AND SULBACTAM — AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0340-2018·2018-02-14

    AuroMedics Recalls Pantoprazole Sodium Injection Due to Glass Particulate

    AuroMedics Pharma LLC is recalling 66,100 vials of Pantoprazole Sodium for Injection because one vial contained a piece of glass.

    Product
    PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0804-2018·2018-02-14

    Panera Chive and Onion Cream Cheese Spread Recalled for Listeria Risk

    Panera, LLC is recalling Chive & Onion Reduced Fat Cream Cheese Spread due to potential Listeria monocytogenes contamination.

    Product
    Panera Chive&Onion Reduced Fat Cream Cheese Spread, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0757-2018·2018-02-14

    Mountain Rose Recalls Prickly Ash Bark Powder Due to Salmonella Risk

    Mountain Rose Inc is recalling Prickly Ash Bark Powder herbal supplements due to potential Salmonella contamination. The product was distributed in 30 states.

    Product
    Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plastic bags depending on quantity ordered, various net weights - 1-oz., 4-oz., 8-oz., 1-lb., 2-lb., 5-lb., 7-lb., 11-lb., 15-lb., and 16-lb. The label is read in parts: "***Prickly…
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Devices)·Z-0508-2018·2018-02-14

    Siemens Artis Biplane Systems Recalled for Ceiling Mount Defect

    Siemens is recalling 265 Artis zee and Artis Q biplane systems because ceiling mount screws may not be fastened correctly.

    Product
    AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0559-2018·2018-02-14

    Recall of Emprint Percutaneous Antenna Due to Tip Disengagement Risk

    FDA is recalling Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm (reinforced), Material CA20L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0558-2018·2018-02-14

    Recall of Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling the Covidien Emprint Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm, Material CA20L1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0326-2018·2018-02-14

    Flawless Beauty Recalls Tatiomax Glutathione Whitening Kits Nationwide

    Flawless Beauty LLC is voluntarily recalling Tatiomax Glutathione Whitening kits nationwide because the products were marketed without FDA approval.

    Product
    Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2018·2018-02-14

    Panera Cream Cheese Recalled Due to Listeria Contamination Risk

    Panera, LLC is recalling Reduced-Fat Plain Cream Cheese (2 oz. and 8 oz.) because it may be contaminated with Listeria monocytogenes. The product was sold nationwide at Panera Cafes.

    Product
    Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·18098·2018-02-14

    ISO Beauty Recalls Ionic Pro Hair Dryers Due to Burn Hazard

    ISO Beauty is recalling Ionic Pro hair dryers because the cord can become brittle, posing a burn hazard. Consumers should stop using the units and contact the company for a refund.

    Product
    Ionic Pro hair dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0560-2018·2018-02-14

    Recall of Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0322-2018·2018-02-14

    FDA Recalls Sterile Morphine Sulfate Preparations Due to Sterility Concerns

    Intrathecal Compounding Specialist, LLC is recalling sterile morphine sulfate preparations compounded between October 16 and November 17, 2017, due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Morphine Sulfate PF Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0328-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Glutathione Injectable Products Nationwide

    Flawless Beauty LLC is voluntarily recalling all lots of Tationil Glutathione and other products sold in kits. The recall is due to misbranding and the sale of unapproved new drugs under a court order.

    Product
    Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettabile, Teofarma, s.r.l.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0321-2018·2018-02-14

    FDA Recalls Hydromorphone Sterile Drug Preparations for Lack of Sterility Assurance

    Intrathecal Compounding Specialist is recalling sterile drug preparations made from Hydromorphone Base Solution due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0332-2018·2018-02-14

    Flawless Beauty Recalls Sterilized Water for Injections Due to Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of sterilized water for injections sold in the U.S. because the products were marketed without FDA approval.

    Product
    Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured in India
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0557-2018·2018-02-14

    Recall of Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA Class II recall of Covidien Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft and remain in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 15cm (reinforced), Material CA15L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0554-2018·2018-02-14

    Mindray TD60 Transmitter Battery Charger Recalled for Overcharging Risk

    Mindray is recalling 203 TD60 Transmitter battery chargers used with the BeneVision Central Station because a damaged circuit board can cause the battery to overcharge and the case to swell.

    Product
    TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
    Category
    Medical Device
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0335-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Glutathione Whitening Injection Kits

    Flawless Beauty LLC is voluntarily recalling all lots of TAD Glutathione Whitening Kits because the products were marketed without FDA approval.

    Product
    TAD Glutathione Whitening Kits lyophilized powder for injection, 600 mg vials, 10 vials + 10 amps x 4 mL, Manufactured by: Biomedica Foscama Industria, Ferentino, Italy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0333-2018·2018-02-14

    Flawless Beauty LLC Recalls Ling Zhi Capsules for Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Ling Zhi capsules because they were marketed without an approved NDA/ANDA, constituting misbranding and unapproved new drugs.

    Product
    Ling Zhi capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0323-2018·2018-02-14

    FDA Recalls Sufentanil Citrate Preparations Due to Sterility Concerns

    The FDA is recalling sterile drug preparations made from Sufentanil Citrate Base Solution due to a lack of sterility assurance. The products were compounded by Intrathecal Compounding Specialists.

    Product
    All sterile drug preparations remaining within expiry prepared from Sufentanil Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide