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 48,124 notices were distributed nationwide, so they reach Oregon too — those are in the archive.

Medical devices

Reported Feb 20, 2013

St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…

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

St Jude Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN. Surgical mesh for use in open or laparoscopic procedures.

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

Allergen Medical

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…

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

Diagnostic Hybrids Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Li-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400. Also branded as Reliability Plus byDrive.…

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

Oxus America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…

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

Synthes USA HQ, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Chocolate Covered Coconut Balls is packaged in either 2-ounce packages (2 pieces per package) or in 0.5 lb and 1 lb.…

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

Chocolate Decadence

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Betty Croker, Super Moist Cake Mix, Golden Vanilla, NET WT 15.25 oz (432 g), UPC 0 16000 40993 4, Dist by General Mills…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 6, 2013

Individual packages labeled in part: ***The Father's Table***Vanilla Roll***8oz**** and Master carton labeled in part:…

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

The Father's Table, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 6, 2013

Kinnikinnick Foods Pie Crusts, 10.2 oz, Item code: 21-35265, UPC 6-20133-00600.

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

Unified Grocers Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2013

Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 23, 2013

Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink.…

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

Ocean Beauty Seafoods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 23, 2013

Brilliance 64 and Ingenuity CT Computed Tomography X-Ray Scanning Systems: Brilliance 64 - Model #728231; and Ingenuity…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2013

Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented…

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

Quanta System, S.p.A.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2013

FlowGate Balloon Guide Catheter; Manufactured by Concentric Medical, Mountain View, CA.…

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

Concentric Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2013

Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R) Phenobarbital Assay (4D019UL). Homogeneous enzyme…

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)

Food

Reported Jan 16, 2013

Udi's gluten free au naturel granola in 12 ounce clear plastic bag, UPC 6-98997-80615-8, best by 041913 12265 1.

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

Udi's Healthy Foods,Granola & Gluten Free

FDA (openFDA food enforcement)

Food

Reported Jan 9, 2013

Fresh Express brand, Fresh Spinach, 9 oz.

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

Fresh Express Incorporated

FDA (openFDA food enforcement)

Medical devices

Reported Jan 9, 2013

Analyzing system consists of a small and portable analyzer and plastic microcuvettes. The microcuvette contains…

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

HemoCue AB

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2013

Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 9, 2013

Hemp Plus Granola. The product is packaged in a 25 lb. container. The UPC is 0 58449 88001 1. The product is labeled in…

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

Nature'S Path Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 2, 2013

Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov,…

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

Arjo, Inc. dba ArjoHuntleigh

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.