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.
Reported Nov 21, 2018
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Wornick Company
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 17, 2018
Swift Beef Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swift Beef Company
USDA FSIS
Reported Nov 14, 2018
Village Baker SPECIALTY ARTISAN BREADS CINNAMON CHIP SOURDOUGH. The product is whole sliced loaves packed in clear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Artisan Baking Company, LLC.
FDA (openFDA food enforcement)
Reported Nov 14, 2018
Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fred Meyer Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2018
FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
New Seasons Market Hot & Sour Broth, packaged in 24 oz glass jar. UPC 840600108672
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Seasons Market LLC
FDA (openFDA food enforcement)
Reported Nov 14, 2018
REF VV19F Reinforced Dual Lumen Cannula, 19Fr., Sterile EO, DISPOSABLE: DO NOT RE-USE CE 0473 Product Usage: The OriGen…
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Acumedia Manufacturers, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1, Class I, 1 Quart (946ml) REF:3306. Product Usage - Impak Elastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CMP Industries, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Medical Incorporated
38 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
S & W White Beans, Net Wt 15 oz (425g), UPC 72273-38807. Distributed by Faribault Foods, 1818 2nd Ave NW, Faribault, MN…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Faribault Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Foodstirs Modern Baking; Organic Minute Mug Cake Mix Celebration Confetti - 4 - 2.54 oz. (72g) Pouches per carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foodstirs
FDA (openFDA food enforcement)
Reported Nov 7, 2018
60% Dark Chocolate Chips, packaged in poly-lined cardboard boxes, net wt. 30 lbs. The label is read in parts: "***…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Portland Chocolate Company LLC
FDA (openFDA food enforcement)
Reported Nov 7, 2018
EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
NucliSENS¿ Magnetic Extraction Reagents
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Oct 31, 2018
BACT/ALERT VIRTUO system, A Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Oregon recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.