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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.

3,339 stored notices name Oregon, reported between Jun 20, 2012 and Nov 11, 2026.

Medical devices

Reported Nov 15, 2023

BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.

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

Breg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260

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

Family Dollar Stores, Llc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Gills Onions 3 lb. bags, diced yellow onions

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

Gills Onions, LLC

72 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP

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

Pulmonx, Corp.

FDA (openFDA device enforcement)

Food

Reported Nov 8, 2023

Nature's Path Organic Pumpkin Spice Waffles, 7 oz., UPC 0 5844959077 4

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

Nature'S Path Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…

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

Betty Lou's Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

SOZO Bilateral Arm L-Dex Software

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

Impedimed Limited

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor

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

Orgain

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental

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

Preat Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

Astral 100 and Astral 150 ventilators

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

ResMed Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 25, 2023

Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 25, 2023

stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502

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

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 18, 2023

Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block…

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

Cardinal Health 200, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 18, 2023

Evivo with MCT Oil Infant Probiotic Activated B. infantis EVC001 (ActiBif) For Enteral or Oral Administration…

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

Infinant Health, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 18, 2023

CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…

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

RoyalVibe Health Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used on the Rotor-Gene Q MDx instrument for the detection…

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

Qiagen GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 4, 2023

Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 4, 2023

1 lb. bags of CellarScience ascorbic acid, packaged in vinyl bags on 11/18/2022, Sku: AD615LB, Batch Number 56559, UPC…

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

Moreflavor, Inc.

FDA (openFDA food 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.