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 Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Defense Nutrition Warrior Whey Natural Powder, dietary supplement, packaged in 14-oz. bottles and packed 6/14-oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Defense Nutrition
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 8, 2012
Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 8, 2012
The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Frozen Oysters are packaged in 8 oz. 40 oz, and 3 lbs. The item numbers are 06413, 03777, FO/HS-OT8; 136300-20110430.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B & F, Inc., dba Hanmi, Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2012
BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bridgepoint Medical
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Leica M525 F50 Surgical Microscope; Article No. 10338422; Leica Microsystems (Schweiz) Ag, 201 Max Schmidheiny Strasse,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
The Handi-Fil Disposable Syringe Fill Tube is a sterile plastic tube, approximately 10 inches in length, with a "J"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mallinckrodt Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tripath Imaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Abbott Molecular Bar Code Scanner User's Guide; instructions for setting up the Bar Code Scanner LN 6L89-01, a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Truitt Brothers, Pacific Northwest Premium Navy Beans, net weight 15 oz. per metal can. The UPC is 0 82225 24145 1. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Truitt Bros., Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Jimmy Peppers Hot Cherry Sliced Peppers, 1 gallon plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cosmo's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Focal SIM Planning of radiation therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.superDimension, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2012
TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 11, 2012
Wheat Germ, brand name PFM, package in bulk tote, approximately 1650 lbs. per tote. Product SKU is 1344.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pendleton Flour Mills, LLC
FDA (openFDA food enforcement)
Reported Jul 11, 2012
Cho-Rip-Dong Frozen Oysters in plastic bags: 1) Item no. BG1501, net wt. 1 lb.; 2) Item no. BG1521, net wt. 8 oz.; 3)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seoul Trading Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 4, 2012
CJ Het Oyster (CJ Frozen Oyster), 40x8oz.. Material#912329, Frozen Oyster (KR 12 SP 050110), Material#912330, Frozen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CJ Foods, Inc., A Division
FDA (openFDA food enforcement)
Reported Jul 4, 2012
BCS(R) Behring Coagulation System, Device catalog No. OVIO03 Product Usage: Multipurpose system for In Vitro…
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)
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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.