All recall categories

Recalls distributed in Oregon

These notices name Oregon 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.

3,297 stored notices name Oregon, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Oregon too — those are in the archive.

Medical devices

Reported Nov 19, 2025

Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The…

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

Shimadzu Corporation Medical Systems Division

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control…

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

Techno-Path Manufacturing Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 12, 2025

SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 12, 2025

Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Truth Cage Free Brown Large AA 12ct; UPC: 011110797698 Stater…

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

Eggs Unlimited LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 12, 2025

Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both…

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

Tandem Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2025

Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software…

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

Aesculap Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles…

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

Alcon Research LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2025

CellMek SPS Sample Preparation System, REF: C44603. Software versions 2.2.122.0 and prior, and Instructions for Use…

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2025

Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test…

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

Cepheid

FDA (openFDA device enforcement)

Medical devices

Reported Nov 5, 2025

ChemoLock Bag Spike, 01 units REF: CL-10-10

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

ICU Medical, Inc.

37 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 29, 2025

Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit"…

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 29, 2025

Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated…

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

Reser's Fine Foods, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 29, 2025

Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats,…

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

Rolling Pin Baking Company LLC

FDA (openFDA food enforcement)

Food

Reported Oct 29, 2025

Frozen Organic Spinach Net Wt. 10 oz (283.5g) poly bags packaged under the following brands: 1. Sno Pac Frozen…

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

Sno Pac Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 29, 2025

Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC:…

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

Southwind Foods LLC dba Great American Seafood Imports Co.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 29, 2025

Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock…

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

Baxter Healthcare Corporation

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167…

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

Cook Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723

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

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The CycloPen…

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

Iantrek Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia.…

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

Sea Port Products Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01…

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

Spacelabs Healthcare, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2025

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and…

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

B Braun Medical Inc.

12 more products in this recall

FDA (openFDA device 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.