All recall categories

Recalls distributed in Washington

These notices name Washington in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,362 stored notices name Washington, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Washington too — those are in the archive.

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 3, 2025

Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CA BOTANA International, Inc.

13 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 3, 2025

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Djo, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

FoundationOne CDx (F1CDx), RAL-0003 version 31.0

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Foundation Medicine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged in flexible plastic bag. UPC 6 09595…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Homeneeds Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

IntelePACS - InteleConnect / TechPortal

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intelerad Medical Systems Incorporated

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mindray DS USA, Inc. dba Mindray North America

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Whatcom Blue Sliced cheese; Sliced and packaged in deli plastic wrap with Whole Foods Scale labels.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

WFM Purchasing, LP

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2025

MONARCH Bronchoscope. Model Number: MBR-000211-B

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Meridian Bioscience, alethia c. Difficile, Catalog Number 480050, Nucleic Acid Amplification Test Assay

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Meridian Bioscience Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name: Olympus Nephro-EZDilate…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Nov 26, 2025

Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Peterson Company Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2025

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant Assay Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Quest International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thoratec LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 26, 2025

Twin Sisters Creamery Whatcom Blue cheese, 2.5lb. round cheese wheel, made with raw milk and aged at minimum of 60…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Twin Sisters Creamery, LLC

3 more products in this recall

FDA (openFDA food enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.