All recall categories

Recalls distributed in Vermont

These notices name Vermont 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.

1,186 stored notices name Vermont, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Vermont too — those are in the archive.

Food

Reported Dec 16, 2020

On the Go Sweet & Salty Trail Mix

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

Kanan Enterprises Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…

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

Hill-Rom Manufacturing, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…

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

Orca Bay Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

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

Thomas Scientific

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2020

Change Healthcare Radiology Solutions 14.0

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

Change Healthcare Canada Company

FDA (openFDA device enforcement)

Food

Reported Oct 14, 2020

SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container

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

Hormel Foods Corporation

FDA (openFDA food enforcement)

Food

Reported Oct 14, 2020

"Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"

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

LuMaZu, LLC dba Nettle Meadow

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2020

PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based,…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2020

NM/CT 850 Model Number: H3907AD

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

GE Healthcare, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 30, 2020

Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9…

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

Gilster-Mary Lee Corp.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 30, 2020

Panther Fusion Tube Tray, Part: FAB-15004, REF: PRD-04000

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2020

The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…

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

Life Technologies Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2020

NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…

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

Novarad Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2020

Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.

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

Hellofresh US

FDA (openFDA food enforcement)

Food

Reported Sep 16, 2020

Blanxart 82% Congo Organic Chocolate Bar. Paper packaging with internal foil wrapper. Net weight per bar: 4.4 oz. UPC 8…

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

Power Selles Imports dba Culinary Collective

FDA (openFDA food 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.