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 Apr 1, 2020

Baskin Robbins Mint Chocolate Chip, Ice Cream Sandwiches with Mint Ice Cream, Semi-Sweet Chocolate Chips & Chocolate…

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

Dean Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is…

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

Hill-Rom Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Enoki Mushroom; Product of Korea; Net Wt. 7.05 oz., (200 g) UPC: 7 426852 625810 The Enoki is packaged in a clear film,…

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

Hong Bin Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

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

Karl Storz Endoscopy

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.

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

Medline Industries Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Red Pozole Soup Starter, Pozole To The People, packaged in glass jars. Net Wt. 16 fl. oz., (473.2 mL). or 24 fl. oz. 16…

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

Proxy Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel…

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

Quidel Cardiovascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

WinCo Foods frozen Blackberries, item # 107414, packaged in polyethylene bags, with a net weight of 16 oz (1 lb or…

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

Winco Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K…

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

Aesculap Implant Systems LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…

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

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044

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

Dreyers Grand Ice Cream, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 25, 2020

Sesame Sticks packaged in clear zip tie 5 oz. bags. UPC 8 40600 11010 1. The FRONT side label is read in parts: "***NEW…

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

New Seasons Market LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

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

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

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

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Monitor for the Functional Imaging System for Magnetic Resonance Imaging System

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device 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.