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.
Reported Jul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2025
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peak Cocktails
FDA (openFDA food enforcement)
Reported Jul 2, 2025
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
DxI 9000 Access Immunoassay Analyzer C11137
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bigfoot Biomedical
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Spectral CT. Computed tomography X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jul 2, 2025
CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preat Corp.
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.RGB Soda, LLC.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Yerba Prima Inc.
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Allon 2001. Part Number: 200-00263
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Belmont Instrument LLC
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Jun 18, 2025
IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Taylor Shellfish Farms Geoduck Chowder Base, frozen, Ingredients: Potatoes, Clam (Geoduck) ***Butter (Cream, Salt),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vern's Foods & Farm
FDA (openFDA food enforcement)
Reported Jun 11, 2025
AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 293070 ##### READY…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
FDA (openFDA food enforcement)
Reported Jun 11, 2025
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Fresh & Ready Foods Breakfast Bistro Box, 4 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89908 9
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh & Ready Foods LLC
85 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 11, 2025
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GNC Holdings LLC
FDA (openFDA food enforcement)
Reported Jun 11, 2025
VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
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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.