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.

Food

Reported Jan 17, 2024

Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7

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

Garden Spot Foods, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…

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

Townsend Design

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

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

Natus Medical Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

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

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111

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

Fresenius Medical Care Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Injection Needle, REF: 25207

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

Karl Storz Endoscopy

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356,…

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

Kenover Marketing Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

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

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

HMC Farms Peaches 2lb Gusset Bag

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

The HMC Group Marketing Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 27, 2023

Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan…

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

Willamette Valley Pie Company, LLC

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157

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

E.A. Sween Co.

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

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

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w

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

Auris Health Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic Acid Test, REF 20-011-018, a…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.

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

Staar Surgical Company

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

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

Thor Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 6, 2023

Bisousweet Confections Chocolate Whoopie Pies

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

Bisousweet Confections

FDA (openFDA food enforcement)

Food

Reported Dec 6, 2023

Bonta Natural Artisan Gelato Stracciatella is frozen dessert, packaged in blue cardboard pint cups (UPC 58745 00309)…

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

Bonta - Natural Artisan Gelato LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

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

Edwards Lifesciences, LLC

5 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.