State

Vermont product recalls

73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22151–22175 of 75495

HighFDA (Devices)·Z-0741-2022·2022-03-16
FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results
Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.
Product
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2022·2022-03-16
B. Braun dispensing pins recalled for air filter leakage risk
B. Braun Medical is recalling dispensing pins with an elevated leakage risk in the air inlet filter. The leakage may reduce medication doses, delay treatment, or contaminate the fluid path, potentially causing bloodstream infection.
Product
Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication or enteral feeding solution from inverted multi-dose vials.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0743-2022·2022-03-16
Medtronic endotracheal tubes recalled due to manufacturing nonconformity
Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.
Product
NIM TRIVANTAGE EMG Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0725-2022·2022-03-16
Philips X-ray System Cooling Leak Poses Fire Risk
Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.
Product
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0732-2022·2022-03-16
Radiation therapy planning software displays wrong images during animation playback
RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.
Product
RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 .…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0724-2022·2022-03-16
Philips Allura Xper X-ray systems cooling system leak poses fire risk
Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.
Product
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2022·2022-03-16
FDA Recalls Diagnostic Test Strips for False Positive Results
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Product
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0739-2022·2022-03-16
Nextra CH Hammertoe Surgical Implant Kit Recalled for Locking Mechanism Defect
Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0729-2022·2022-03-16
Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications
A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.
Product
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22103·2022-03-16
B. toys Wooden Activity Walker recalled for choking hazard
B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.
Product
B. toys Wooden Activity Walker - Walk 'n' Learn
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V162000·2022-03-16
2021 Volkswagen ID.4 Battery Cell Soldering Defect Recall
Volkswagen is recalling certain 2021 ID.4 vehicles due to improper soldering of the high-voltage battery connection. The defect may cause an unreliable connection that could lead to vehicle stalling and increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0823-2022·2022-03-16
El Chavito Saladitos Enchilados Salted Plums Recalled for Potential Lead Contamination
El Chavito Saladitos Enchilados Salted Plums (1.7 oz.) are being recalled nationwide due to potential lead contamination. Consumers should not consume this product.
Product
El Chavito¿ Saladitos Enchilados Salted Plums with Chili, net wt. 1.7 oz., Individual UPC 859470006070, Master Case UPC 859470006612.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0740-2022·2022-03-16
Surgical hammertoe instruments recalled for potential locking mechanism deformation
The Nextra Cannulated Hammertoe Standard Instrument Kit's driver may deform the implant locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22099·2022-03-16
Reckitt Recalls 3.74 Million Bottles of Airborne Gummies for Pressure Hazard
RB Health (Reckitt) is recalling approximately 3.74 million bottles of Airborne Gummies (63 and 75 count) because pressure buildup can cause the cap and seal to pop off with force upon first opening, posing an injury hazard.
Product
Airborne Gummies (63 and 75 count bottles)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0735-2022·2022-03-16
Laboratory diagnostic tips recalled for potential dispensing errors
Ortho-Clinical Diagnostics is recalling VITROS Chemistry VersaTips due to shape deformity that may reduce sample volume by 16%. Undetected errors could result in inaccurate test results for bloodborne infectious disease assays.
Product
VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0822-2022·2022-03-16
El Chavito Saladitos Dried Salted Plums Recalled for Potential Lead Contamination
El Chavito Saladitos Dried Salted Plums are being recalled due to potential lead contamination. The recall affects 37,552 packages distributed nationwide.
Product
El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag, Individual UPC 859470006049, Master Case UPC 859470006629. El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag, Individual UPC 850013297221, Master Case UPC 850013297726.
Category
Food
Distribution
Distributed nationwide
HighCPSC·22104·2022-03-16
Prestone Shop Pro RV & Marine Antifreeze Recall for Methanol Poisoning Risk
Prestone has recalled Shop Pro RV & Marine Antifreeze sold at AutoZone after discovering some bottles were improperly filled with methanol-containing product and lack required hazard warnings. Methanol can cause poisoning through inhalation or ingestion and may be fatal or cause blindness.
Product
Shop Pro RV & Marine Antifreeze
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0728-2022·2022-03-16
Stryker Camera Control Unit Recalled Due to Inverted Image Display Defect
Stryker is recalling the 1688 Camera Control Unit due to a software defect that causes the surgical monitor image to flip upside-down. This could lead to surgeon error or the need for additional surgical intervention.
Product
1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy, and plastic surgery wherever a laparoscope/endoscope/arthroscope/sinuscope is used.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0746-2022·2022-03-16
PCA 4000 Dental Curing Units May Not Fully Cure Resins
Envisiontec is recalling 172 PCA 4000 curing units that may not properly cure dental resins to specification (SKU ACC-06-1000).
Product
PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22100·2022-03-16
Specialized Bicycle Crank Arm Disengagement Recall Poses Fall Hazard
Specialized is recalling about 19,000 Sirrus bicycles with defective alloy cranks that can disengage and cause falls. The manufacturer has received 30 reports of the defect, but no injuries have been reported.
Product
Sirrus, Sirrus X and Sirrus Sport Bicycles with alloy cranks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22102·2022-03-16
RH Illuminated Mirrors Recalled Due to Fire and Shock Hazards
RH is recalling about 3,300 illuminated mirrors sold from September 2015 through February 2022 due to loose components in bulb sockets that can cause overcurrent, overheating, fire, and electrical shock. Consumers should stop using them immediately and contact RH for a refund or replacement.
Product
Illuminated Mirrors
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V160000·2022-03-16
Harley-Davidson Motorcycles Recalled for Detaching Brake Fluid Warning Labels
Harley-Davidson is recalling certain 2021-2022 XL Sportster motorcycles because brake fluid warning labels may detach from reservoir caps. Missing labels could lead to improper brake maintenance and increased crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON XL883N, XL1200X, XL1200NS
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0649-2022·2022-03-16
Paliperidone Extended-Release Tablets Recalled for Failed Dissolution
The Harvard Drug Group is recalling 174 cartons of Paliperidone Extended-Release Tablets, 9 mg, nationwide due to failed dissolution specifications. The affected lots are N00522 (Exp. 09/2022) and N00618 (Exp. 11/2022).
Product
PALIPERIDONE — PALIPERIDONE (PALIPERIDONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0723-2022·2022-03-16
CIRRUS HD-OCT Optic Nerve Angiography Feature Requires Deactivation
Carl Zeiss Meditec is recalling CIRRUS HD-OCT Models 5000 and 6000 AngioPlex devices. The optic nerve head angiography feature was distributed without FDA pre-market clearance and must be disabled.
Product
CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0744-2022·2022-03-16
PuraSinus Nasal Hemostat Recalled Due to Unvalidated Shipping Boxes
3-D Matrix, Inc. is recalling PuraSinus Absorbable Nasal Hemostat units because the shipping boxes used for transport were not validated.
Product
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
Category
Medical Device
Distribution
Distributed nationwide