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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.

Medical devices

Reported Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

NuVasive Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2022

Red Button Vintage Creamery French Silk Pie, Net Wt. 31.88 oz. (904g), in a clear plastic dome and black plastic base,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rocky Mountain Pies, LLC

FDA (openFDA food enforcement)

Food

Reported Dec 21, 2022

Sardines in tomato sauce packed in cans labeled in part, "WILD PACIFIC SARDINES RAINCOAST TRADING TM***IN TOMATO…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intersect ENT, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GS Biomark LLC

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Hill-Rom Progressa Bed System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2022

Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2022

Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2022

Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Avanos Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

iRhythm Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2022

BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company, BD Biosciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bella Brands, LLC dba Bella Cucina Artful Food

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 9, 2022

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

Food Club Chive Cottage Cheese, 16 oz; Hannaford Chive Cottage Cheese, 16 oz; Hood Chive Cottage Cheese, 16 oz and 24…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HP Hood LLC

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 9, 2022

THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

TASTE OF INSPIRATION 8 oz Brie - w/Herb center layer, rounds UPC 725439802567

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Old Europe Cheese, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 2, 2022

CorVocet Biopsy System/Catalog Code: CORA1610/B, CORA1610S/B, CORA1615/B, CORA1810/A, CORA1810/B, CORA1810S/B,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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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.