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 Mar 3, 2021
Aaron's Gourmet Smoked Fish (King, Sockeye, or Steelhead) packaged in glass jars or in vacuum plastic bags. The label…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aaron's Gourmet Smoked Fish
FDA (openFDA food enforcement)
Reported Mar 3, 2021
Infusion Pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Mar 3, 2021
Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ecolab Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
Brite Harbor Caesar Dressing & Dip, 1.5 oz pillows (pouches), item # 16002. The front label states "***BRITE HARBOR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Litehouse Inc.
FDA (openFDA food enforcement)
Reported Mar 3, 2021
VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
ENROUTE Transcarotid Stent System REF SR-XXYY-CS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silk Road Medical Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
OT1000 Series Orthopedic Surgical Tables
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Feb 24, 2021
Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confirm Biosciences Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2021
System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
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 Feb 17, 2021
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draegar Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
"LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Evr Foods Inc.
FDA (openFDA food enforcement)
Reported Feb 10, 2021
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Dole Endless Summer Salad Kit; 13 oz. bag UPC: 0-71430-01073-0 Contains Milk, Wheat Distributed by Dole Fresh…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Feb 10, 2021
Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…
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 Feb 3, 2021
Dole Chopped Kit Sesame Asian Salad & Topping Net Wt: 9.5 oz (269 g) Dressing Net: 2.5 FL oz (72 mL) Total Net Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Feb 3, 2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
32 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
JTM FOOD GROUP brand READY TO EAT WHITE CHEDDAR MACARONI & CHEESE in 5 lb. plastic bags, 6 bags per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JTM Provisions Co. Inc.
FDA (openFDA food enforcement)
Reported Jan 27, 2021
Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
AnshLabs - SARS-CoV2 IgM ELISA (u-Capture), IVD, REF: AL-1002, kit contents, Ab PLATE 1 X ! Plate, IgM Sample DIL 1 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansh Labs, LLC
FDA (openFDA device enforcement)
Reported Jan 20, 2021
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
5 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.