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.

Medical devices

Reported Aug 28, 2024

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever…

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

Inari Medical - Oak Canyon

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2024

Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged in 8 oz. PET plastic bottles; UPC 0-78742-29655-5

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

Refresco Beverages US Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 28, 2024

Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

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

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Cepheid, Sample Collection Device, Part: 900-0370

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

Cepheid

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid…

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

Merit Medical Systems, Inc.

22 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test

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

Luminex Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

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

Hoff & Pepper, Co. LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2024

Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner,…

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

Medivance Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025

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

Prophet Premium Blends, LLC

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2024

Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

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

Abbott Medical

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…

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

C. Krueger Finest Baked Goods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…

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

Echonous Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 3, 2024

2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401,…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504),…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2024

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2024

The Synchro Neuro Guidewires are a steerable guidewire family with a shapeable tip. The outside diameter of the Synchro…

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

Stryker Neurovascular

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

BD Pyxis MedStation ES, REF: 323, Medication Cabinet

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

CareFusion 303, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 29, 2024

Sammy's Milk GOAT MILK TODDLER FORMULA, 25.68 oz (78g) pouch

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

Graceleigh, Inc. dba Sammy's Milk

1 more product 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.