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 Mar 23, 2022

All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in…

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

The Royal Ice Cream Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2022

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

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

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2022

Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mixed fruit and popping boba with sweetened juice. 3.5 0z (4…

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

Del Monte Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 16, 2022

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

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

Factor

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2022

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

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

Acorn Stairlifts, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2022

Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6…

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

J & M Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 2, 2022

Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…

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

Medtronic Vascular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 2, 2022

NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R

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

Nobel Biocare USA LLC

FDA (openFDA device enforcement)

Food

Reported Feb 16, 2022

Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 2, 2022

Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually

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

Brownie Points LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 26, 2022

ARIES HSV 1&2 Assay, Part Number/REF 50-10017

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 12, 2022

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

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

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…

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

AMO Manufacturing USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…

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

Activbody, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…

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

Fujifilm Irvine Scientific, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 17, 2021

NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…

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

NOW Health Group Inc.

2 more products in this recall

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.