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 Sep 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Plum administration sets

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

ICU Medical, Inc.

7 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software…

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

Nuclein LLC

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Philips Patient Information Center iX REF:866389

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

Philips North America

1 more product in this recall

FDA (weekly enforcement report)

Food

Reported Sep 23, 2026

Diced Jalapenos. Ingredients: Jalapeno Pepper. Net Wt: 3.75 oz. Keep Refrigerated. Distributed by: Taylor Farms Inc.,…

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

Taylor Fresh Foods Inc.

24 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

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

Baxter Healthcare Corporation

19 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 2, 2026Updated Sep 13, 2026

Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…

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

Byron White Formulas, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540,…

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

Arrowhead DE LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…

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

Covidien, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7

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

Gifford's Dairy, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

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

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

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

SDI Limited

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 26, 2026

Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of…

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

Shanghai Ravioli Corporation

USDA FSIS

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

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

Erbe USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

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

OBP Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20;…

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

Boston Scientific Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

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

Permobil Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…

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

ResMed Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2026

functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…

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

Nutricia North America

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 15, 2026

Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…

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

Hamilton Medical AG

1 more product in this recall

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.