The Recall Desk

State

Washington product recalls

73,100 recalls have nationwide distribution and so reach Washington. 8,459 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,459
Critical
867
Severe
2,008
Most recent
2026-09-23

Of the 8,459 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,008 (24%) are Severe.

These figures cover only the 8,459 recalls whose distribution notice names Washington specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9676–9700 of 81559

  • HighCPSC·25030·2024-11-07

    Dreamgro Lullaby Travel Soothers Recalled Due to Choking Hazard

    Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.

    Product
    Dreamgro Lullaby mermaid travel soothers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25032·2024-11-07

    Guava Roam strollers recalled due to brake failure and fall hazards

    Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.

    Product
    Guava Roam Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25033·2024-11-07

    Baofali 4-in-1 Microfiber Crib Bumpers Recalled for Suffocation Hazard

    Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.

    Product
    Baofali 4-in-1 Microfiber Crib Safety Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V842000·2024-11-07

    Micro Bird Recalls 2023 CT-Series Buses Due to Ignition Interlock Defect

    Micro Bird is recalling 2023 CT-Series buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V839000·2024-11-07

    2022-2023 Chevrolet Express and GMC Savana transmission software defect

    GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0088-2025·2024-11-06

    Reser's Caesar Salad Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Caesar Salad Kits due to Listeria monocytogenes contamination in the cooked chicken component. The recall affects 21,098 cases distributed across 31 U.S. states.

    Product
    Item 401311, UPC 13454 35855, Caesar Salad Kit 2/6 lbs. Distributed by Fresh Creative Foods Vista, CA.
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Food)·F-0089-2025·2024-11-06

    Ginger Chicken Broccoli Salad Kit Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Ginger Chicken Broccoli Salad Kit V due to potential Listeria monocytogenes contamination in the cooked chicken. The product was distributed to 31 states.

    Product
    Item 404790, UPC 13454 38101, Ginger Chicken Broccoli Salad Kit V, 1/6.9625lb. Distributed by Fresh Creative Foods Vista, CA.
    Category
    Food
    Distribution
    30 states
  • SevereNHTSA·24V837000·2024-11-06

    PJ TRAILERS LD trailers recalled for incorrectly installed brake axles

    PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.

    Product
    PJ TRAILERS — PJ TRAILERS LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0092-2025·2024-11-06

    VasoView HemoPro Vessel Harvesting System Recalled for Silicone Component Detachment

    Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.

    Product
    VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0120-2025·2024-11-06

    Shirakiku Korean Seaweed Recalled for Undeclared Sesame Allergen

    Wismettac Asian Foods recalls Shirakiku Korean Seasoned Seaweed due to incorrect product labeling that fails to disclose sesame. Affected products were distributed in CA, AZ, TX, NM, WA, NY, and NV.

    Product
    The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as follows: (Principal Display Panel) Roasted Seaweed 10-0.91 OZ (26 G) PACKAGES (NET WT 9.1 OZ (260 G). (Back Display) ROASTED SEAWEED Organic Yaki Nori Ingredient
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0267-2025·2024-11-06

    Nihon Kohden SpO2 Sensor Recalled Lacking FDA Market Approval

    Nihon Kohden America is recalling its Adult/Pediatric Forehead Disposable SpO2 Sensor (Model 809030006) because the device was distributed without FDA market approval or clearance.

    Product
    Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult, 10/Box
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Drugs)·D-0026-2025·2024-11-06

    Cinacalcet tablets recalled for manufacturing impurity exceeding FDA limits

    Dr. Reddy's Laboratories recalls Cinacalcet 30 mg tablets nationwide due to manufacturing defects that produced N-nitroso impurity above FDA recommended limits. Patients should contact their healthcare provider if they are taking an affected lot.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0264-2025·2024-11-06

    Olympus Electrosurgical Generator ESG-410 Recalled for Audio Buffer System Error

    Olympus Corporation recalls 279 units of its ESG-410 electrosurgical generator nationwide due to increased complaints of system error E1226 (Could not write to Audio Buffer) occurring during surgical procedures.

    Product
    Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0244-2025·2024-11-06

    Surgical patties and strips recalled for elevated endotoxin levels in raw materials

    Integra LifeSciences has recalled Codman surgical patties and strips due to higher-than-expected endotoxin levels in raw materials, which may result in out-of-specification endotoxin in finished products.

    Product
    SURG PAT XRAY 1/2X2 Model/Catalog Number: 801406. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0257-2025·2024-11-06

    Covidien Chameleon PTA Balloon Catheter Recalled for Failed Pressure Testing

    Covidien is recalling specific lots of its Chameleon PTA Balloon Catheter that failed in-house pressure testing. The affected catheters were distributed worldwide to the US and 18 countries.

    Product
    Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm x 75cm (CFN CH05-40-75US), 6mm x 40mm x 75cm (CFN CH06-40-75US), 7mm x 40mm x 75cm (CFN CH07-40-75US), 8mm x 40mm x 75cm (CFN CH08-40-75US), 9mm x 40mm x 75cm (CFN CH09-40-75US), 10mm x 40mm x 75cm (CFN CH10-40-75US),
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0078-2025·2024-11-06

    Bistro 28 Chicken Enchilada Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Bistro 28 Creamy Green Chile Chicken Enchilada Meal Kits due to Listeria monocytogenes contamination in the cooked chicken. The affected meal kits were distributed across 30 U.S. states.

    Product
    Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready in 5 MIN. Net wt. 27 oz (1 LB 11 OZ) 765g. Distributed by Fresh Creative Foods, Vista, CA. Case GTIN 10013454384937, Case UPC 13454 38493, Bistro 28 Creamy Gre
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0246-2025·2024-11-06

    Surgical Patties and Strips Recalled for Elevated Endotoxin Levels

    Codman Surgical Patties and Strips are being recalled due to higher-than-expected endotoxin levels in raw materials. Approximately 93,782 units were distributed worldwide for use in protecting tissue during surgery.

    Product
    SURG PAT XRAY 1X3 Model/Catalog Number: 801408. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0270-2025·2024-11-06

    Laryngeal Tube Device Recalled for Unapproved Pediatric Indication

    King Systems Corp. is recalling 21,939 KING LTSD laryngeal tubes nationwide because the device was marketed for pediatric use without proper FDA regulatory clearance. The device was originally approved only for adult use.

    Product
    KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD421
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0080-2025·2024-11-06

    Bistro 28 Chicken Burrito Bowl Express Meal Kit recalled for Listeria

    Reser's Fine Foods is recalling Bistro 28 Chicken Burrito Bowl Express Meal Kits distributed across 31 states due to Listeria monocytogenes contamination in the cooked chicken. No illnesses have been reported.

    Product
    Item 407119, UPC 13454 38494, Bistro 28 Chicken Burrito Bowl Express Meal Kit. Ready in 5 MIN. Net wt. 25 oz (1 LB 9 OZ) 788g. Distributed by Fresh Creative Foods, Vista, CA. Case GTIN 10013454384944, Case UPC 13454 38494, Bistro 28 Chicken Burrito Bowl Express Meal Kit. 4/25oz.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0092-2025·2024-11-06

    Reser's Asian Style Stir Fry Meal Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling 420 cases of Asian Style Stir Fry meal kits containing potentially contaminated cooked chicken due to Listeria monocytogenes. Affected products were distributed across 30 states with Use By dates from September through November 2024.

    Product
    Item 406897,UPC 13454 38407, Asian Style Stir Fry Single Serve OP no Trays 1/6.5 LB. Distributed by Fresh Creative Foods, Vista, CA.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0087-2025·2024-11-06

    Premium Street Taco Kit Meal Recalled for Listeria Monocytogenes

    Reser's Fine Foods is recalling Premium Street Taco Kits due to Listeria monocytogenes contamination in the cooked chicken. Approximately 4,100 cases were distributed across 30 states.

    Product
    Item 404700, UPC 13454 38075, Premium Street Taco Kit With Trays, 2/4.9875 lbs. Distributed by Fresh Creative Foods Vista, CA.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0252-2025·2024-11-06

    Surgical Patties and Strips Recalled for Endotoxin Contamination

    Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw material, which may result in out-of-specification endotoxin in finished products.

    Product
    SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0228-2025·2024-11-06

    Hospital Bed Fails to Send Remote Alerts Through Nurse Call System

    Hillrom Centrella Smart+ hospital beds may fail to send remote alerts through the Rauland Responder 5 Nurse Call System, though local bed alerts still function. This could delay nursing staff notification of patient needs.

    Product
    a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed, Product codes: P7900B000001, P7900B100010, P7900B100024, P7900B100208, P7900B100273, P7900B100304, P7900B000005, P7900B100011, P7900B100025, P7900B100212, P7900B100277, P7900B100307, P7900B000010, P7900B100017, P7900B10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0261-2025·2024-11-06

    Ambu VivaSight 2 DLT endotracheal tubes recalled for hyper angulation risk

    Ambu is recalling VivaSight 2 DLT endotracheal tubes due to hyper angulation of the distal end, which increases risk of intubation complications and airway injury.

    Product
    Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 412391000), 41 Fr (Catalog Number 412411000)
    Category
    Medical Device
    Distribution
    Distributed nationwide