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 May 6, 2020

Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen; Software version 02.00.00.0076 - Product Usage: The…

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

Obalon Therapeutics Inc.

FDA (openFDA device enforcement)

Food

Reported May 6, 2020

5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink

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

Ocean Spray Cranberries Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2020

Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and…

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

Philips North America, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2020

Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…

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

Welch Allyn, Inc/mortara

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 6, 2020

Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in…

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

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Apr 29, 2020

ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express…

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

Beckman Coulter Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Nitinol Thermocouple Electrode, 10 cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of…

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

Boston Scientific Neuromodulation Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Canon Aquilion Lightning, Model TSX-036A

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

Canon Medical System, USA, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 22, 2020

Roasted/Salted Deluxe Mixed Nuts; Net Wt. 10 oz./284 g, Clear plastic container UPC 65143370994 Cashews, Almonds,…

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

DSD Merchandisers, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2020

Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin for Gases and Electrolytes

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

Smiths Medical ASD, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

The CF-70 instrument (product code: LXG; Regulation Number: 862.2050) receives magazines containing stained blood…

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

Sysmex America, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastomosis of veins and…

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.

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

Biomet, Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)

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

Lindt & Sprungli (USA), Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2020

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

PRIVATE SELECTION FROZEN BERRY MEDLEY in 16 oz. (10 bags per case) and 48 oz. bags (6 bags per case). UPC: 0001111079120

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Nature's Blend Folic Acid 1000 mcg Dietary Supplement, 1000-count bottle, Product Number: 1280, UPC 0-79854-51280-9

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

National Vitamin Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the…

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

Ra Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

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

Respironics California, LLC

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2020

NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087562088, Packaged…

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

Vitamin Cottage Natural Food Markets, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…

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

Bard Peripheral Vascular Inc.

9 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.