All recall categories

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.

Medical devices

Reported May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

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

Allergan Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The…

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

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported May 8, 2024

Bottle is labeled as Johnny's Parmesan Garlic Seasoning, 5oz (141g), packaged in poly bottle with green spice cap, UPC…

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

OS Holding Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly

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

Thoratec Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

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

Quidel Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional…

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

Route 92 Medical Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the…

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

XENEX Disinfection Services Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2024

Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates,…

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

Canadian Art Prints

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2024

Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,

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

Masimo Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.

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

SonarMed Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 17, 2024

Taylor Farms Buffalo Chicken Party Tray, packaged in black plastic tray with clear plastic lid. This tray consists of 9…

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

Taylor Farms Northwest, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 10, 2024

ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2024

Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only

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

Karl Storz Endoscopy

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2024

Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for…

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2024

Epix Universal Clip Applier, REF: CA500, STERILEEO

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

Applied Medical Resources Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2024

Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C

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

Medivance Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 3, 2024

Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle

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

Nordic Naturals, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 3, 2024

Product LAbeled in part: "Emerald River Premium Thai Jasmine Rice ... Net Wt 50 lb (22.7 kg) ... UPC 0 28571 00474 6"

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

Otis McAllister

FDA (openFDA food enforcement)

Medical devices

Reported Mar 27, 2024

Liquid Protein Calibrators. C3 and Haptoglobin liquid protein calibrators used with Randox IgA, IgG, and IgM assays…

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

Randox Laboratories Ltd.

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.