State

Vermont product recalls

73,576 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total: 2,011
Critical: 209
Severe: 531
Most recent: 2026-10-21

Of the 2,011 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 2,011 recalls whose distribution notice names Vermont specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26126–26150 of 75587

HighFDA (Devices)·Z-1299-2021·2021-03-31
Meridian ImmunoCard Mycoplasma EIA Recalled for Potential False-Negative Results
Meridian Bioscience is recalling 8 ImmunoCard Mycoplasma EIA kits due to incorrect storage that could cause false-negative or invalid results, potentially delaying appropriate patient treatment.
Product
The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of recent Mycoplasma pneumoniae infection.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2021·2021-03-31
Mizuho Operating Table Hand Control Units Recalled for Sliding Risk
Mizuho OSI is recalling 26 operating table hand control units because they may cause the tabletop to slide in the opposite direction, potentially delaying surgical procedures.
Product
Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2021·2021-03-31
In2Bones Shannon Percutaneous Burr Recalled for Potential Breakage During Use
In2Bones is recalling 60 units of Shannon Percutaneous Burrs due to manufacturing non-conformity that may cause the burr to break during surgery.
Product
In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1290-2021·2021-03-31
Corin Trinity Hip Prosthesis Heads Recalled for Incorrect Size Labeling
Corin Ltd is recalling 23 units of Trinity Biolox Delta Ceramic Heads due to incorrect size labeling on packaging and patient stickers.
Product
Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1301-2021·2021-03-31
Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the product to stick, preventing proper application.
Product
In-View Clear Leggings Sterile Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1304-2021·2021-03-31
Cardinal Health Recalls Femoral Angiography Drapes Due to Sticking Defect
Cardinal Health is recalling non-sterile femoral angiography drapes because a manufacturing defect causes them to stick, preventing proper application.
Product
Femoral Angiography Drape Bulk Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1300-2021·2021-03-31
Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings Sterile because a manufacturing variance causes the plastic film to stick, potentially preventing proper application.
Product
In-View Clear Leggings Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1279-2021·2021-03-31
Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability
Baxter Healthcare is recalling 1,650 Prismaflex Control Units used for renal replacement therapy because tubing performance variability may cause alarms during or after system self-tests.
Product
Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1303-2021·2021-03-31
Cardinal Health Recalls Sterile Femoral Angiography Drapes Due to Sticking Defect
Cardinal Health is recalling 936 units of sterile femoral angiography drapes because a manufacturing variance causes the plastic film to stick, preventing proper application.
Product
Femoral Angiography Drape Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1291-2021·2021-03-31
Corin Trinity Acetabular System Recalled for Incorrect Size Labeling
Corin Ltd is recalling 23 units of the Trinity Acetabular System because the size indicated on the packaging and patient stickers is incorrect.
Product
Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1302-2021·2021-03-31
Cardinal Health Recalls In-View Clear Leggings Due to Sticking Defect
Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the plastic film to stick, preventing proper application.
Product
In-View Clear Leggings Bulk Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1295-2021·2021-03-31
Ortho-Clinical Diagnostics Recalls VITROS TIBC Calibrator Kits Due to Performance Shift
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 4 and Fe Slides because TIBC results may be approximately 80 ug/dL lower than expected.
Product
VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC only). Used to calibrate VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems Product Code: 1204668 Impacted Products: A. VITROS Chemistry Products TIBC Kit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1277-2021·2021-03-31
Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability
Baxter Healthcare is recalling Prismaflex Control Units because tubing variability may cause alarms during self-tests. The units are used for Continuous Renal Replacement Therapy.
Product
Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1288-2021·2021-03-31
Siemens Recalls 29 Interventional Fluoroscopic X-Ray Systems for Shutdowns
Siemens is recalling 29 interventional fluoroscopic X-ray systems because the power supply may cause the computer to shut down unexpectedly.
Product
Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V220000·2021-03-30
Dennis Eagle Elite and Proview Recalled for Incorrect ABS Warning Light
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because the ABS warning light may illuminate incorrectly when brake pads wear out, potentially causing driver confusion.
Product
DENNIS EAGLE — DENNIS EAGLE PROVIEW, ELITE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E024000·2021-03-30
Cummins Recalls Electric Drivetrain Parts Due to High Voltage Shock Risk
Cummins is recalling Electric Drivetrain part number PD7000 because it cannot detect isolation faults, posing a high voltage shock risk to service personnel.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:SHOCK PROTECTION recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V223000·2021-03-30
2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure
Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.
Product
LINCOLN — LINCOLN AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V221000·2021-03-30
2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy
2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.
Product
ALFA ROMEO — ALFA ROMEO STELVIO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V222000·2021-03-30
Pierce Recalls 2016-2018 Trucks Due to Excessively Bright Rear LED Lights
Pierce Manufacturing is recalling 2016-2018 Enforcer, Freightliner, and Saber trucks because rear LED lights may be too bright, potentially blinding other drivers.
Product
PIERCE — PIERCE FREIGHTLINER, ENFORCER, SABER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E023000·2021-03-30
Nado LED Headlight Bulb Recall for Excessive Glare and Brightness
Nado Stuff is recalling MICTUNING LED headlight bulbs that create excessive glare, increasing crash risk. Owners will receive a full refund.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21E022000·2021-03-30
BEAMTECH LED Headlight Bulbs Recalled for Excessive Glare and Brightness
Guangzhou Lengzhilu Trading Co., Ltd. is recalling specific BEAMTECH LED headlight bulbs because they create excessive glare, failing federal safety standards.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V218000·2021-03-29
Winnebago Recalls 2020 Minnie RVs Due to Incorrect Tire Labeling
Winnebago is recalling 2020 Minnie vehicles because the Tire and Loading Information label lists the wrong tire size, which could lead to improper tire installation and increased crash risk.
Product
WINNEBAGO — WINNEBAGO MINNIE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V219000·2021-03-29
2021 Forest River Berkshire Class A Motorhomes: Brake Light Reflection Defect
Forest River is recalling certain 2021 Berkshire Class A motorhomes due to brake lights that may not adequately reflect light. The defect affects visibility and compliance with Federal Motor Vehicle Safety Standards.
Product
FOREST RIVER — FOREST RIVER BERKSHIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V217000·2021-03-26
Mercedes-Benz Recalls AMG Models Due to Starter Cable Fire Risk
Mercedes-Benz is recalling 493 AMG E63S and GT63 models because an incorrectly installed starter cable may chafe wires, causing a short circuit, vehicle stall, or fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, AMG GT63, AMG GT63S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V216000·2021-03-26
2020 Mercedes-Benz E-Class passenger seat limiter safety recall
Mercedes-Benz is recalling certain 2020-2021 E-Class and AMG models due to a passenger seat limiter defect that may allow the seat to position too close to the frontal airbag, increasing injury risk during airbag deployment.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, E63 AMG, E 350, AMG E53
Category
Vehicle
Distribution
Distributed nationwide