The Recall Desk

State

Washington product recalls

72,940 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 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 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4876–4900 of 81396

  • HighNHTSA·25V745000·2025-10-30

    2025 Kia Telluride and 2026 Sorento Spare Tire Assembly Recall

    Kia is recalling certain 2025 Telluride and 2026 Sorento vehicles due to an incorrect spare tire that can impair the anti-lock braking and traction control systems, increasing crash risk.

    Product
    KIA — KIA TELLURIDE, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V744000·2025-10-30

    Toyota, Lexus, and Subaru vehicles with defective panoramic rearview camera

    Toyota Motor Engineering & Manufacturing is recalling 2022–2026 Toyota, Lexus, and Subaru vehicles with a Panoramic View Monitor system due to a software error that may freeze or blank the rearview camera in reverse, reducing rear visibility and increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA, SUBARU TX PLUG-IN HYBRID, redundant RX PLUG-IN HYBRID, NX HYBRID, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·26057·2025-10-30

    Glow stick bracelets recalled because green bracelet can leak and irritate

    About 6,600 Destination Holiday Glow Light Stick bracelet 12-packs are being recalled because the green bracelet can leak, posing a skin irritation hazard.

    Product
    Destination Holiday Glow Light Stick Bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0088-2026·2025-10-29

    Deli pasta salad recalled because it may contain Listeria monocytogenes

    Sprouts Farmers Market is recalling Smoked Mozzarella Pasta Salad sold at deli counters and in grab-and-go containers because the product may contain Listeria monocytogenes.

    Product
    Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers at Deli counter and into 16oz plastic grab & go containers, weight dependent on customer request, UPC 2-15587-00000 (from service case) and 2-15786-00000 (from
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·H-0089-2026·2025-10-29

    Spinach free bowtie pasta kits recalled over potential Listeria contamination

    Reser's Fine Foods is recalling 795 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags of affected Bowtie Pasta and does not contain spinach. Kit is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-0091-2026·2025-10-29

    Penne salad kits recalled over potential Listeria monocytogenes contamination

    Reser's Fine Foods is recalling 4,770 cases of Fresh Creative Foods Smoked Mozzarella Penne Salad Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404284 Smoked Mozzarella Penne Salad Kit, UPC #13454 37904. Perishable/Refrigerated product. Net wt. 13lbs. This kit contains 2/3lbs. sealed bag of affected Penne Pasta and kit is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-0132-2026·2025-10-29

    Shrimp scampi meals recalled over linguine linked to Listeria outbreak

    Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.

    Product
    Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0136-2026·2025-10-29

    Impella controllers recalled over purge pressure issues from retainer failures

    Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.

    Product
    Automated Impella Controller (AIC) labeled as the following with corresponding Product Codes: 1. AIC w/Impella Connect for ECP, Product Code: 1000432. 2. Dbl optical, AIC Impella Connect, Phg US, Product Code: 1000201. 3. Impella Controller, Packaged, AU, Product Code: 0042-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0094-2026·2025-10-29

    Basil pesto bowtie salad recalled over recalled pasta ingredient and Listeria

    Kroger is recalling 5,567.4 lbs of Basil Pesto Bowtie Pasta Salad because the store-made deli item contains a pasta ingredient recalled for potential Listeria monocytogenes.

    Product
    Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fr
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·H-0149-2026·2025-10-29

    Breakfast burritos recalled after cooked egg ingredient tested positive for Listeria

    M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.

    Product
    Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0154-2026·2025-10-29

    IV burette sets recalled over missing internal shutoff valve component

    ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.

    Product
    IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0070-2026·2025-10-29

    Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors

    B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.

    Product
    Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0095-2026·2025-10-29

    Kroger penne salad recalled over Listeria in recalled pasta ingredient

    Kroger is recalling 25,792 lbs of store-made Smoked Mozzarella Penne Salad because it contains a pasta ingredient recalled for potential Listeria monocytogenes.

    Product
    Smoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli service counters) or UPC 227573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·H-0150-2026·2025-10-29

    Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria

    M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.

    Product
    Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0090-2026·2025-10-29

    Bowtie pasta kits recalled over potential Listeria monocytogenes contamination

    Reser's Fine Foods is recalling 3,252 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bowtie Pasta, and it is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·25V737000·2025-10-29

    Mazda CX-50 front suspension bolts may allow wheel detachment

    Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.

    Product
    MAZDA — MAZDA CX-50, CX-50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0236-2026·2025-10-29

    BACTEC FX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0112-2026·2025-10-29

    Frozen cooked shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0240-2026·2025-10-29

    Veritor Connect software recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0210-2026·2025-10-29

    Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0227-2026·2025-10-29

    Bipolar hip heads recalled downstream after femoral components failed transit testing

    Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.

    Product
    iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2026·2025-10-29

    PVC stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0114-2026·2025-10-29

    Frozen cooked salad shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0215-2026·2025-10-29

    Clinical analyzer modules recalled over dilution factor software anomaly affecting results

    Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.

    Product
    DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0113-2026·2025-10-29

    Frozen raw shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen raw shrimp sold under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen Raw shrimp; 2lbs; 1lbs; UPC: 041130810923; 041512179471; 041130810978; 041130811029; 011110641182; 829944010636; 041130811333; 041130810916; 041130812460; 041130810824; 829944012463; 829944012012; 829944004079
    Category
    Food
    Distribution
    34 states