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 Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Candela Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Jansal Valley brand Indulgent Snack Mix NET WT 12 OZ (340 G) in plastic clamshells, Ingredients: apricots, almonds,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Fruit Market dba Sid Wainer & Son
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 23, 2019
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
BD FACSLyric Flow Cytometer, 2-Laser 4 Color Instrument, REF: 662875, when using BD Trucount Tubes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Consider Bardwell Farm brand Slyboro Handmade Goat Cheese - Ingredients Raw Goat Milk, Cultures, Salt, Microbial Rennet…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Consider Bardwell Farm, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 16, 2019
FSIS Issues Public Health Alert for Beef Products due to Possible E. coli O157:H7 Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Oct 16, 2019
Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Udi's Classic Hamburger Buns, packaged in a 10.4 oz. plastic bag, with eight bags per wholesale case. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConAgra Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PreGel America, Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2019
ABL90 FLEX Analyzer REF 393090 UDI:05700693930909
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device 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.