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 Jul 22, 2026
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2026
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Jul 22, 2026
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix U.S. LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh & Ready Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 15, 2026
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Think Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2026
GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wallac Oy
FDA (openFDA device enforcement)
Reported Jul 8, 2026
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mars Snacking
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 8, 2026
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026Updated Sep 16, 2026
Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diagnostics Scarborough, Inc.
FDA (weekly enforcement report)
Reported Jul 1, 2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Dried Herring Fish 7 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Food Processing LLC.
FDA (openFDA food enforcement)
Reported Jul 1, 2026
INZONE DETACHMENT SYSTEM, REF: M00345100950
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 1, 2026
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Foods, LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 25, 2026
FSIS Issues Public Health Alert for Boneless Chicken Breast Product Due to Misbranding and Undeclared Allergens
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.FW Farms LLC.
USDA FSIS
Reported Jun 24, 2026
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arrow International, LLC
34 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.