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.

1,205 stored notices name Vermont, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Vermont too — those are in the archive.

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

iLet Bionic Pancreas, REF: BB1001

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

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Mito Red Light, Super Mobile

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

Mito Red Light Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2026

Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2026

Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52…

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

HF Acquisition Co. LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…

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

Kico Knee Innovation Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…

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

Becton, Dickinson and Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros;…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported May 20, 2026

Swad Orange Flavored Masala Candy

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

Raja Foods and Vegetables Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2026

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…

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

Erbe Medical, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 13, 2026

SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI NET WT. 25 LBS. ORIGEN: ARGENTINA EXPORTADOR: ESPAR SRL…

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

Falcon Trading Co., Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 13, 2026

french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…

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

French Broad Chocolate Factory

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2026

Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 13, 2026

Garland Fresh Peeled Garlic 6 oz. bag

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

Tops Markets LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported May 13, 2026

LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family…

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

Wehah Farms

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

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

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2026

Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…

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

Blueroot Health, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 15, 2026

Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is…

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

Riverence Provisions LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Vermont recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.