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 Oct 20, 2021
Endoskeleton" TAS Interbody System with Titan nanoLOCK" Surface Technology, Nanolock 12 Dg Interbody, Large, 12mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CardioQuip, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Djo, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deerfield Imaging, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Sep 29, 2021
DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Sep 29, 2021
EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Sep 22, 2021
BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Arjo Disposable Repositioning Sling, Model AHD001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Dominican Republic SA
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic pouch, sliced on a coated board, 24 packages to a case. UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Loki Fish Company - Office
FDA (openFDA food enforcement)
Reported Sep 22, 2021
Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Naturo Aid Pharmaceutical Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 15, 2021
Pipeline Flex Embolization Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc.,
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 15, 2021
Trader Joe's Super Spinach Salad with Quinoa, carrots, cranberries, chickpeas, edamame, pumpkin seeds and a carrot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Class Distribution, Inc.
FDA (openFDA food enforcement)
Reported Sep 8, 2021
Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
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.