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 Dec 6, 2023

Da Vinci Single-Site Wristed Needle Driver, REF: 478115, 5 mm

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K…

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

Convergent Dental

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

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

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

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)

Free recall alerts

Get alerted about new Oregon recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.