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.
3,339 stored notices name Oregon, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Oregon too — those are in the archive.
Reported Oct 4, 2023
Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with four independent RF channels, allowing all RF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Great Lakes Cheese, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Liquid Assayed Chemistry Control Premium Plus Level 3, Catalog Number LAE4215
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2023
For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Sep 13, 2023
ZVU Functional GI Software, REF: ZVU-3
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diversatek Healthcare
FDA (openFDA device enforcement)
Reported Sep 13, 2023
FSIS Issues Public Health Alert for Kirkland Signature Chicken Tortilla Soup Product Due to Misbranding
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kettle Cuisine Midco, LLC
USDA FSIS
Reported Sep 13, 2023
ISee Ortho-K Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PARAGON VISION SCIENCES, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the Radixact Treatment Delivery System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2023
Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Real Kosher Ice Cream, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2023
Newly Weds Foods R03810 LOEFFLER COMP PORK ROLL CURE X1 54lbs
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Newly Weds Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2023
Tim Heung Yuen Black Melon Seed 6 oz., 12 oz. Ingredients: Melon Seeds, Salt, Sugar & Anise Seed Distributed By Richin…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Richin Trading Inc.
FDA (openFDA food enforcement)
Reported Aug 16, 2023
FABRIQUE' EN CORSE TOMME CORSE AU LAIT DE BREBIS***ANTOINE OTTAVI FROMAGER***aFFINAGE 3 A' 5 MOIS SARL Fromagerie…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Estancia Holdings
FDA (openFDA food enforcement)
Reported Aug 9, 2023
Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
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.