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 Aug 26, 2026Updated Sep 7, 2026

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

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

Paragonix Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

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

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

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

SDI Limited

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2026Updated Sep 7, 2026

Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…

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

529 Commerce, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

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

Erbe USA Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2026Updated Aug 25, 2026

Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE.…

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

FlavorsandColor.Com

FDA (openFDA food enforcement)

Food

Reported Aug 19, 2026Updated Sep 16, 2026

Lyle Style Hot and Spicy Bloody Mary Mix, 32oz. glass bottle. UPC code 7 84762 03770 9. The label declares…

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

Lyle Style

FDA (weekly enforcement report)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

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

OBP Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

GM Helix Implant, Endosseous Dental Implant Article No. 109.984

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

Straumann USA LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 12, 2026

Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics…

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

Cheer Pack

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2026

Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530…

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

Maquet Critical Care AB

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…

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

Pride Mobility Products Corp.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 12, 2026

Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720.…

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

PT Organics Limited

FDA (openFDA food enforcement)

Medical devices

Reported Aug 5, 2026

L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…

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

Argon Medical Devices, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

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

Permobil Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…

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

ResMed Ltd.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 30, 2026

FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Mary's Harvest Fresh Foods, Inc.

USDA FSIS

Medical devices

Reported Jul 29, 2026

Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only.…

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

Ferno-Washington Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT

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

Penumbra, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 24, 2026

Maple Leaf Foods Inc. Recalls Not Ready-To-Eat (NRTE) Bacon Product Imported without the Benefit of Import Reinspection

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

Maple Leaf Foods Inc.

USDA FSIS

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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.