State

Vermont product recalls

73,503 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total: 2,009
Critical: 209
Severe: 531
Most recent: 2026-09-23

Of the 2,009 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 531 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23201–23225 of 75512

SevereFDA (Food)·F-0230-2022·2021-12-08
Jumbo Yellow Onions Recalled for Possible Salmonella Contamination
Onions 52 is recalling 40-pound cartons of Jumbo Yellow Onions imported from Chihuahua, Mexico, due to possible contamination with Salmonella Oranienburg. The recall is voluntary and covers products distributed nationwide and in select regions.
Product
40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico - Label Carzalia Valley Produce, Distributed by Carzalia Valley Produce, Columbus, NM. UPC 00815222010023 Imported from Chihuahua, Mexico, sourced from ProSource and shipped from July 1, 2021 through August 25, 2021.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0265-2022·2021-12-08
Pfizer 5% Dextrose Injection Recalled for Potential Bag Leakage
Pfizer is recalling one lot of 5% Dextrose Injection (50 mL ADD-Vantage Units) due to lack of sterility assurance; the bags have the potential to leak. This is a Class II recall affecting 765 bags distributed nationwide.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V946000·2021-12-08
Western Star 4900 Recalled for Steering Shaft Pinch Bolt Issue
Daimler Trucks North America is recalling 2021-2022 Western Star 4900 vehicles because the steering shaft pinch bolt may not be properly tightened, risking loss of steering control.
Product
WESTERN STAR — WESTERN STAR 4900
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0228-2022·2021-12-08
Jumbo Red Onions recalled for possible Salmonella contamination
Onions 52 is voluntarily recalling 5-pound cartons of Jumbo Red Onions labeled Imperial Fresh due to possible Salmonella Oranienburg contamination. The onions were imported from Chihuahua, Mexico and distributed nationwide.
Product
5# (LB) Ctn (box) Jumbo Red Onions, Product of Mexico - Label Imperial Fresh Distributed by Carzalia Valley Produce, Columbus, NM. UPC 1039494. Imported from Chihuahua, Mexico, sourced from ProSource and shipped from July 1, 2021 through August 25, 2021. Store in cool dry…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·21V945000·2021-12-08
2022 Thomas Built SAF-T-LINER C2 School Buses: Gas Pedal Misalignment Risk
Daimler Trucks North America is recalling 2022 Thomas Built SAF-T-LINER C2 school buses because the gas pedal assembly may be misaligned and wear through the floor mat, potentially trapping the pedal and causing unintended acceleration.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0286-2022·2021-12-08
Sandoz Enoxaparin Sodium Injection Recalled Due to Temperature Excursion
Sandoz Inc. is recalling 45,036 cartons of Enoxaparin Sodium Injection USP 40 mg/0.4 mL due to temperature abuse during shipping. The affected lot was distributed nationwide.
Product
Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only; 0.4 mL Syringes, Manufactured for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-02; Carton (10 x 0.4 mL Syringes), Manufactured by Shenzhen…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0229-2022·2021-12-08
Medium Red Onions Recalled for Possible Salmonella Contamination
Onions 52 is voluntarily recalling Medium Red Onions imported from Chihuahua, Mexico due to possible contamination with Salmonella Oranienburg. The affected products were distributed nationwide.
Product
12 count per 2 lb. mesh sacks with UPC 033383 601014 Medium Red Onions Product of Mexico Farm Fresh Label Distributed by Onions 52 Carrollton, TX. 12 count per 3 lb. mesh sacks with UPC 033383 601021 Medium Red Onions Product of Mexico Farm Fresh Label Distributed by Onions 52…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·21V947000·2021-12-08
Audi SQ5 and Q5 recalled for water ingress into control module
Volkswagen Group of America (Audi) is recalling certain 2018–2022 Audi Q5 and SQ5 vehicles. Water or liquid can seep into the gateway control module, causing sudden engine power loss and increasing crash risk.
Product
AUDI — AUDI Q5, SQ5, Q5 SPORTBACK
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22027·2021-12-08
Mark of Fifth Avenue Children's Robes Recalled for Flammability Hazard
Mark of Fifth Avenue children's robes do not meet federal flammability standards for sleepwear and pose a risk of burn injuries. About 10,000 units sold online at Amazon and Walmart from August 2019 through June 2021 are affected.
Product
Children's robes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0321-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss
Boston Scientific is recalling Hurricane RX dilation balloons used in endoscopic biliary procedures due to pinhole defects causing pressure loss that may prolong treatment.
Product
HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0327-2022·2021-12-08
FDA Recalls Hurricane RX Dilation Balloons for Pressure Failure Risk
Boston Scientific is recalling Hurricane RX Dilation Balloons nationwide due to pinhole defects that cause pressure loss or failure to maintain pressure during endoscopic procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545960
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2022·2021-12-08
Siemens Dimension Vista 500 software issue affects test accuracy
Siemens is recalling 1,326 Dimension Vista 500 diagnostic devices worldwide due to incorrect default hemolysis, icterus, and lipemia indices that may affect test result accuracy.
Product
Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10284473 (US) and 10488224 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0315-2022·2021-12-08
INBONE Total Ankle System recalled for package-labeling mismatch
Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.
Product
INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0320-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloons Recalled for Pressure Loss Defect
Boston Scientific is recalling specific lots of Hurricane RX Dilation Balloons due to a pinhole defect that causes pressure loss, resulting in prolonged endoscopic procedures. Affected devices are used for dilating strictures in the bile duct.
Product
HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545890
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0322-2022·2021-12-08
Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect
Boston Scientific is recalling the Hurricane RX Dilation Balloon due to a pinhole defect causing pressure loss during endoscopic procedures. The defect may result in prolonged procedures and inability to effectively treat biliary strictures.
Product
HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:M00545910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0330-2022·2021-12-08
Dimension Vista 1500 Diagnostic Device: Incorrect HIL Index Defaults
Siemens is recalling 1,407 Dimension Vista 1500 diagnostic devices worldwide due to incorrect default Hemolysis, Icterus, and Lipemia (HIL) index values affecting five assays.
Product
Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10444801(US) and 10444802 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2022·2021-12-08
UV-C Germicidal Wand Recalled for Excessive Ultraviolet-C Radiation
MAX LUX CORP is recalling approximately 9900 handheld UV-C germicidal wands (Safe-T Lite) distributed nationwide due to excessive ultraviolet-C radiation emissions.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0242-2022·2021-12-08
Target Good & Gather Mixed Berry Sparkling Water Recall for Unlabeled Sulfites
Target Good & Gather Mixed Berry Sparkling Water in 8-packs is being recalled due to unlabeled sulfites. Keurig Dr Pepper discovered the issue after receiving complaints about off flavor and off aroma.
Product
Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pack): 0 85239 11345 5
Category
Food
Distribution
Distributed nationwide
HighCPSC·22028·2021-12-08
GE Appliances Recalls Free-Standing and Slide-In Ranges for Tip-Over Hazard
GE Appliances is recalling approximately 132,000 free-standing and slide-in electric and gas ranges because they can tip over if a heavy object is placed on an open oven door and the anti-tip-over bracket is not securely installed, risking burn injuries.
Product
Free-Standing and Slide-In Electric and Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0326-2022·2021-12-08
Boston Scientific HURRICANE RX Dilation Balloon Recalled for Pressure Loss
Boston Scientific is recalling HURRICANE RX Dilation Balloons due to a pinhole defect that causes pressure loss during endoscopic procedures. The device may fail to maintain necessary pressure, potentially prolonging procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0241-2022·2021-12-08
Target Good & Gather Coconut Pineapple Sparkling Water Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because some cans contain unlabeled sulfites. The affected products were distributed nationwide.
Product
Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239 03833 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0312-2022·2021-12-08
Blood Culture Identification Test Recalled Due to False Positive Risk
BioFire Blood Culture Identification 2 (BCID2) diagnostic panels are being recalled due to increased risk of false positive Acinetobacter calcoaceticus-baumannii results caused by non-viable contamination in blood culture vials.
Product
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog No./Description: 442023/BD BACTEC Plus Aerobic medium in plastic vials 442021/BD BACTEC Lytic Anaerobic medium in plastic vials 442192//BD BACTEC Plus Aerobic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0328-2022·2021-12-08
Cholesterol test system recalled due to calibration failure
RANDOX CHOL cholesterol test system is recalled due to a calibration defect that causes quality control results to be flagged as out of range. This could result in inaccurate cholesterol measurements in patient samples.
Product
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0318-2022·2021-12-08
Blood collection devices recalled due to premature needle retraction
Magnolia Medical Technologies is recalling Steripath Gen2 Blood Collection Systems due to an uptick in complaints of premature needle retraction during blood collection.
Product
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0239-2022·2021-12-08
7UP Zero Sugar Lemon Lime Soda Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling 7UP Zero Sugar Lemon Lime Soda due to unlabeled sulfites detected after customer complaints about off flavor and aroma. The recall affects 9,152 cases distributed nationwide.
Product
7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790
Category
Food
Distribution
Distributed nationwide