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.
Reported Jun 21, 2023
Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 Version A, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2023
Vital Proteins Collagen Peptides, retail 24oz plastic canister, UPC 8 57273 00866 6; 6 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Proteins
FDA (openFDA food enforcement)
Reported May 31, 2023
Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
truCONTROL 60 Count
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruVision Health LLC
11 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2023
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZB Importing LLC
FDA (openFDA food enforcement)
Reported May 10, 2023
SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Apr 26, 2023
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Apr 5, 2023
ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Ish Company
FDA (openFDA food enforcement)
Reported Mar 29, 2023
BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2023
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Ultracell Wick with 80cc Collection Bag, 20/box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec International, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Companion Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Brava, 20 oz, 22 ct/case and Brava, 24 oz, 18 ct/case frozen pizza dough
Moderate riskThis product could cause temporary or reversible health problems — stop using it.It'll Be Pizza, LLC.
6 more products in this recall
FDA (openFDA food enforcement)
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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.