The Recall Desk

State

Washington product recalls

73,722 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.

Which agencies issued them

These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30151–30175 of 82257

  • SevereFDA (Food)·F-1599-2020·2020-10-07

    Spokane Produce Recalls Sliced Onions Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling sliced red onions because they may be contaminated with Salmonella Newport. The product was distributed in Idaho, Montana, Oregon, Washington, and Wyoming.

    Product
    Item 78750 Onion Red Sliced, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label. Item 78751 Onion Red Sliced, Refrigerated, net wt. 5 LB, packaged in Sealed Plastic Bag. No label. Item 78701 Onion Red Sliced Tray, Refrigerated, net wt. 5 LB, packaged…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1612-2020·2020-10-07

    Spokane Produce Recalls Stew Mix Trays Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling refrigerated stew mix trays because they contain onion supplied from a source associated with Salmonella Newport.

    Product
    Item 80849 Stew Mix Trays, Refrigerated, net wt. 24 OZ, packaged in Plastic Container. Label does not have cooking instructions.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0045-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,253 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. This defect could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30" GS-20 CV9975G, UDI: 20884521149585 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3053-2020·2020-10-07

    ESAOTE Portable Ultrasound AC/DC Power Supply Recall for Overheating Risk

    ESAOTE is recalling AC/DC power supplies for specific portable ultrasound systems because the connector may heat up, generate smoke, and melt.

    Product
    AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC Adapter associated with the following portable ultrasound diagnostic systems: The AC/DC adapter is intended for use with the following portable ultrasound systems: MyLabAlpha…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1560-2020·2020-10-07

    Spokane Produce Recalls Epicurean Greek Salad Kits Due to Salmonella Risk

    Spokane Produce, Inc. is recalling Epicurean Greek Salad Kits because they contain onion supplied from Thomson International, Inc., which is associated with Salmonella Newport.

    Product
    Item 80631, Epicurean Greek Salad Kit, Refrigerated, net wt. 8.4 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0015-2021·2020-10-07

    Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling non-sterile Velosorb sutures that could compromise sterile fields and increase infection risk.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30" V-20 Taper, Product Number: CV417G, UDI: 20884521149370 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1585-2020·2020-10-07

    Spokane Produce Recalls Pico De Gallo Salsa Due to Salmonella Risk

    Spokane Produce, Inc. is recalling two items of refrigerated Pico De Gallo Salsa Hot because they contain onion supplied from Thomson International, Inc. that may be contaminated with Salmonella Newport.

    Product
    Item 83985 Pico De Gallo Salsa Hot, Refrigerated, net wt. 8 OZ, packaged in Plastic Container. Item 83986 Pico De Gallo Salsa Hot Saddlin' Up, Refrigerated, net wt. 16 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0007-2021·2020-10-07

    FDA Recalls Endo GIA Auto Suture Units Due to Staple Formation Defects

    FDA is recalling Endo GIA Auto Suture Universal Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.

    Product
    Endo GIA Auto Suture Universal Loading Unit, Item Code 030457 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0031-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,264 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" KV-11, TaperCutting, Product Number: CV2293, UDI: 20884521151588 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21003·2020-10-07

    Endliss Recalls Trianium Battery Phone Cases Due to Burn Hazard

    Endliss Technology is recalling Trianium battery phone cases because the lithium-ion batteries can overheat and cause burns. Consumers should stop using them and contact the company for a replacement.

    Product
    Trianium cell phone battery pack cases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0030-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,262 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-14, Product Number: SVP2251, UDI: 20884521177380 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1553-2020·2020-10-07

    Spokane Produce Recalls Parisian Kale Salad Kits Due to Salmonella Risk

    Spokane Produce, Inc. is recalling refrigerated Parisian Kale Salad Kits because they contain onion supplied from Thomson International, Inc. that may be contaminated with Salmonella Newport.

    Product
    Item 80194 Parisian Kale Salad Kit, Refrigerated, net wt. 4.25 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0024-2021·2020-10-07

    blumen Clear Advanced Hand Sanitizer Recalled for CGMP Deviations

    4e Brands North America is recalling blumen Clear Advanced Hand Sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor Current Good Manufacturing Practices.

    Product
    blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 7.5 fl oz / 221 ml bottle, UPC 8 14266 02362 4 c) 15.2 fl oz (450 ml) bottle, UPC 8 14266 02392 1, d) 17 fl oz / 503 ml bottle with blue…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0049-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 9,214 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" C-13 Cutting SV2298, UDI: 20884521151021 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1578-2020·2020-10-07

    Spokane Produce Recalls Fresh Medium Salsa Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling 8-ounce containers of Fresh Medium Salsa because the product contains onion supplied by Thomson International, Inc., which is associated with Salmonella Newport.

    Product
    Item 84023 Fresh Medium Salsa, Refrigerated, net wt. 8 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0034-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,811 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36" GS-25, Product Number: CV605, UDI: 20884521152295 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Blumen Advanced Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.

    Product
    blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3052-2020·2020-10-07

    ESAOTE AC/DC Power Supply Recall for Portable Ultrasound Systems

    ESAOTE is recalling AC/DC power adapters for specific portable ultrasound systems because the connector may heat up, smoke, or melt due to mechanical stress.

    Product
    AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC Adapter associated with the following portable ultrasound diagnostic systems: The AC/DC adapter is intended for use with the following portable ultrasound systems: MyLabAlpha…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0002-2021·2020-10-07

    Sun Pharmaceuticals Recalls RIOMET ER Due to NDMA Impurity

    Sun Pharmaceuticals is recalling RIOMET ER (metformin hydrochloride) oral suspension because it contains the impurity NDMA.

    Product
    RIOMET ER (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL 16 oz. For Oral Use Only Rx Only Manufactured by: Sun Pharmaceuticals Industries Limited Mohali, India Distributed by: Sun Pharmaceuticals Industries, Inc. Cranbury, NJ 08512 NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0028-2021·2020-10-07

    Modesa Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Modesa hand sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor manufacturing practices.

    Product
    Modesa instant HAND SANITIZER with moisturizers & vitamin E, (70% ethyl alcohol), 33.8 FL OZ (1 L) bottle, Distributed by Greenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320, Made in Mexico. UPC 0 32251 49935 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1619-2020·2020-10-07

    365 Organic Reduced Fat Popcorn Recalled for Glass Contamination

    Eagle Family Foods is recalling 365 Organic Reduced Fat Popcorn because pieces of glass may be present in the product.

    Product
    365 Whole Foods Market Organic Reduced fat &Sodium Popcorn, 6 oz. bag, UPC 099482435349, 10 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Blumen Advanced Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.

    Product
    blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural Boost with Tea Tree Oil, (70% ethyl alcohol), Packaged as a) 18 fl oz / 532 ml bottle, UPC 8 14266 02408 9 b) 33.8 fl oz / 1L bottle, UPC 8 14266 02374 7, Distributed in USA and Canada BY: 4e Brands…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1555-2020·2020-10-07

    Spokane Produce Recalls Refrigerated Black Bean Salad Kits Due to Salmonella

    Spokane Produce, Inc. is recalling 261 pounds of refrigerated Southwest Black Bean Salad Kits because they may be contaminated with Salmonella Newport.

    Product
    Item 80634 Southwest Black Bean Salad Kit, Refrigerated, net wt. 8.7 LB, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0008-2021·2020-10-07

    Endo GIA Stapler Recall Due to Incomplete Staple Formation

    FDA recalls Endo GIA Auto Suture staplers because staples may not form properly, potentially preventing adequate hemostasis during surgery.

    Product
    Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm, Item Code 030458 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide