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 48,122 notices were distributed nationwide, so they reach Oregon too — those are in the archive.

Medical devices

Reported Sep 20, 2017

Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use.…

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

Leica Biosystems Richmond Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2017

Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 13, 2017

MOSAIQ Medical Charged-Particle Radiation Therapy System

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2017

OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0…

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

Litehouse Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 6, 2017

CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.

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

Gold Medal Products Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…

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

Optovue, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 30, 2017

Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

Gold Coast Packing Broccoli Florets; packed in the following configurations: 12 x 2 lb - Product code 508215 - Costco…

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

Fresh Venture Foods, LLC

FDA (openFDA food enforcement)

Food

Reported Aug 30, 2017

SKU 081223, Trader Joes Asian Stir Fry, 12/18 oz packages, UPC 812238 Ingredients Statement: Green Pepper, Broccoli,…

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

Mary's Harvest Fresh Foods, Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

Rainbow Carrot and Quinoa Salad, ready to eat product, packaged in one pint clear plastic deli containers, sold at…

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

New Seasons Market

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.

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

Shippert Medical Technologies

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…

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

Cyberonics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 23, 2017

Kettle Brand Krinkle Cut Potato Chips Spicy Queso, 8.5 oz., Distributed by: Kettle Foods, Inc., Salem, OR 97301, UPC:…

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

Kettle Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2017

iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 9, 2017

Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point brand. Product is packaged in a plastic tray with heat sealed…

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

Nisbet Oyster Co. Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 9, 2017

Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…

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

Professional Complementary Health Formulas, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2017

Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 2, 2017

Bateman Recalls Poultry Products Due To Misbranding and an Undeclared Allergen

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

Bateman

USDA FSIS

Medical devices

Reported Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 230 V

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

Sorin Group USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 26, 2017

FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS; UPC: 7 28028 44036 2

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

Fit and Focused Supplements

FDA (openFDA food enforcement)

Food

Reported Jul 26, 2017

Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173

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

J F C International Inc.

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.