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 May 25, 2022
VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz, 2x8x18 oz Clamshell Distributed by Strawberry Associated,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Driscoll's Inc.
FDA (openFDA food enforcement)
Reported May 25, 2022
Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported May 25, 2022
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Total Resources Intl
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
New Seasons Market Truffle Valencia Almonds, packaged in a round plastic tub with lid, sold by various weights.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Seasons Market LLC
FDA (openFDA food enforcement)
Reported May 18, 2022
Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported May 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snak King Corporation
FDA (openFDA food enforcement)
Reported May 11, 2022
K-Wire, 1.35 mm x 170 mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 11, 2022
Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular procedures. Used to shunt blood at the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 11, 2022
TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported May 6, 2022
Olympia Meats Recalls Ready-To-Eat Pork Deli Meat Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olympia Provisions
USDA FSIS
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported May 4, 2022
groundwork MIND-FULL Bar. Ingredients: Gluten-free oats, Flax seed, Chocolate chips, Brown sugar, Chia seeds, peanut…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Groundwork Coffee LLC
FDA (openFDA food enforcement)
Reported May 4, 2022
da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2022
TearCare version 1.0 SmartHubs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Sciences, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2022
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DNA Genotek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
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.