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.
Reported Oct 24, 2012
MJM Tropical Treats, Tropical Shaped Grahams, Orange, Net Wt. 1 oz., MJM Marketing, Super Wholesome Grahams, P.O. Box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richmond Baking
FDA (openFDA food enforcement)
Reported Oct 17, 2012
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Gourmet Firm Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Northwest Tofu, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 17, 2012
Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R) Phenobarbital Assay (4D019UL) Product Usage: Enzyme n…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Fruit Medley - 1) Zupan's brand Island Medley 12 oz UPC 92504723497 2) Mary's Select brand Island Fruit Medley - 12 oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.United Salad Company
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 10, 2012
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Animas Corporation
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Cucina Fresca Smoked Tomato Sauce. Product is packaged in a glass jar, net weight 24 oz. The UPC is 8-84337 00522-4
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cucina Fresca, Inc.
FDA (openFDA food enforcement)
Reported Oct 10, 2012
BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invuity, Inc.
FDA (openFDA device enforcement)
Reported Oct 10, 2012
VA Kit New Gourmet Fruit Salad 7.75#. Item # 70006, UPC is 0 20728 70006 8. Label reads in part "***VA KIT NEW GOURMET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pacific Coast Fruit Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 10, 2012
Champ's Sliced White Mushrooms, 227 g/8 oz, in a styrofoam container with shrink wrap, UPC 0 33383 67600 5. Labeled in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spokane Produce, Inc.
FDA (openFDA food enforcement)
Reported Oct 10, 2012
Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2012
DEXIS Imaging Suite - catalog number 1.008.7932, version numbers 10.0.0 through 10.0.3 Radiological Image Processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imaging Sciences International, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Invacare¿ I-Fit" Shower Chair (Models 9780, 9781, 9781-1), Invacare Corporation, Elyria, OH 44035. These shower chairs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 3, 2012
UltraFlow HPC Flow Directed Micro Catheter, Model # 105-5065. Product Usage: The UltraFlow HPC Flow Directed Micro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics Inc., dba Ev3 Neurovascular
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2012
SharePlan 1.1, aka t-RayAutoplan version 1.2.1 (build number 1.3.1.10). Manufacturing name RayAutoplan, aka…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Fruit Mixes: 1) Dining In¿ Super Fruit Medley,10.5oz, UPC 1122508396, Use by date 9/6/2012; 2) Ready Pac¿ Super Fruit…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ready Pac Foods Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2012
Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Precise Digital Accelerator Delivery of radiation to defined target volumes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haag-Streit USA Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hocean Inc.
FDA (openFDA food enforcement)
Reported Sep 26, 2012
The 2.7mm Drilling Guide is a reusable instrument used in conjunction with a drill to prepare oriented holes in bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra Life Sci.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
2 more products in this recall
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.