The Recall Desk

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.

26151–26175 of 75587

  • SevereCPSC·21732·2021-03-25

    Polaris Recalls Ranger and Utility Vehicles Due to Fire Hazard

    Polaris is recalling approximately 41,500 Ranger, ProXD, Gravely, and Bobcat off-road vehicles because a drive belt can break, damage the fuel line, and cause a fire.

    Product
    Model Year 2020-2021 RANGER 1000 and RANGER CREW 1000, Model Year 2020 ProXD 2000G and 4000G, Model Year 2020-2021 Ariens/Gravely JSV3200, JSV3400, and JSV6400, Model Year 2020 Bobcat UV34 4x4 GAS and UV34 XL GAS, and Model Year 2021 Bobcat UV34 4x4 GAS
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V214000·2021-03-25

    RV Chassis steering column defect may cause loss of steering

    Shyft Group is recalling certain 2021-2022 Spartan RV Chassis K1-K4 vehicles. A steering column defect may cause the steering output shaft to disengage, resulting in loss of steering control and crash risk.

    Product
    SPARTAN — SPARTAN K3, K4, K2, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V215000·2021-03-25

    Honda and Acura Recall Vehicles for Fuel Pump Failure Risk

    Honda is recalling 2018-2020 Acura and Honda vehicles because the fuel pump may fail, causing the engine to stall while driving.

    Product
    ACURA — ACURA, HONDA TLX, RDX, CR-V, CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V210000·2021-03-25

    2021 Chevrolet Tahoe seat belt latch may be inaccessible

    GM is recalling certain 2021 Chevrolet Tahoe vehicles because the second-row center seat belt latch may be trapped beneath the trim bezel. Passengers cannot use this seat belt, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V213000·2021-03-25

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Steering Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because a poor electrical connection may cause loss of power steering, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V211000·2021-03-25

    Chevrolet Camaro 2017-2021 Air Bag Emblem Separation Recall

    General Motors is recalling certain 2017-2021 Chevrolet Camaro vehicles because the plastic 'Camaro' emblem on the steering wheel air bag cover may separate during air bag deployment, creating a projectile hazard.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21733·2021-03-25

    KTM, Husqvarna, and GASGAS Recall Competition Motorcycles Due to Crash Hazard

    KTM, Husqvarna, and GASGAS are recalling about 1,470 model year 2021 closed course competition motorcycles because the drive chain can break, posing a crash hazard.

    Product
    KTM, Husqvarna and GASGAS closed course competition motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V212000·2021-03-25

    2021 Ducati Multistrada engine valve defect increases crash risk

    Certain 2021 Ducati Multistrada V4 S motorcycles may have excessive valve guide wear that could break the valve head, decreasing engine performance and increasing crash risk. Ducati will replace the affected motorcycle engines at no cost.

    Product
    DUCATI — DUCATI MULTISTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1195-2021·2021-03-24

    Medtronic Custom Perfusion Pack Recalled for Bacterial Endotoxin Levels

    Medtronic is recalling 4 units of Custom Perfusion Packs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Perfusion Pack (CUSTOM PACK HY11B40R1 1/4 RESPIRATO). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1196-2021·2021-03-24

    Medtronic Affinity Pixie Cardiotomy Reservoir Recalled for Bacterial Endotoxin

    Medtronic is recalling 70 units of Affinity Pixie Cardiotomy/Venous Reservoirs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filtered, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1190-2021·2021-03-24

    Medtronic Affinity Pixie Oxygenator Recalled for Bacterial Endotoxin

    Medtronic is recalling Affinity Pixie Oxygenators due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses in patients.

    Product
    Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous Reservoir with Balance Biosurface (OXYGENATOR BBP241 AFFINITY PIXIE WCVR OU). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1199-2021·2021-03-24

    Medtronic Recalls Custom Perfusion System Due to Endotoxin Risk

    Medtronic Perfusion Systems is recalling 7 units of the Custom Perfusion System because they may contain elevated levels of bacterial endotoxins, which can cause acute inflammatory responses in patients.

    Product
    Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filtered, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1194-2021·2021-03-24

    Medtronic Affinity Pixie Cardiotomy Reservoir Recalled for Bacterial Endotoxin

    Medtronic is recalling 10 units of the Affinity Pixie Cardiotomy/Venous Reservoir due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V200000·2021-03-24

    Porsche Recalls 2021 Models Due to Engine Connecting Rod Defect

    Porsche is recalling 2021 Cayman, Boxster, and 718 Spyder vehicles because engine connecting rods may crack and loosen, increasing the risk of a crash or fire.

    Product
    PORSCHE — PORSCHE redundant CAYMAN, redundant BOXSTER, 718 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V204000·2021-03-24

    Jayco Recalls 2019-2020 Motorhomes Due to Gas Leak Risk

    Jayco is recalling 2,144 motorhomes because a stove component may cause a gas leak, increasing the risk of fire.

    Product
    ENTEGRA — ENTEGRA, JAYCO ESTEEM, ODYSSEY, REDHAWK, GREYHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V203000·2021-03-24

    Starcraft RV Recalls 2019-2020 Travel Trailers Due to Gas Leak Risk

    Starcraft RV is recalling 2019-2020 travel trailers because an overtightened bolt may damage a seal, causing a gas leak that increases fire risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH OUTFITTER, MOSSY OAK, MOSSY OAK LITE, AUTUMN RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1191-2021·2021-03-24

    Medtronic Affinity Pixie Oxygenator Recalled for Bacterial Endotoxin

    Medtronic is recalling 57 units of Affinity Pixie oxygenators due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous Reservoir with Balance Biosurface (OXYGENATOR BBP241 W/CVR NI BB STERILE). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1192-2021·2021-03-24

    Medtronic Recalls Custom Perfusion System Due to Endotoxin Risk

    Medtronic Perfusion Systems is recalling three units of its Custom Perfusion System because they may contain elevated levels of bacterial endotoxins. Patients exposed to these devices could develop an acute inflammatory response.

    Product
    Custom Perfusion System (CUSTOM PACK HY10J00R6 ECC SMALL CAR). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filtered…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0303-2021·2021-03-24

    Spironolactone Tablets Recalled Due to Potential Labeling Error

    Bryant Ranch Prepack is recalling 35 bottles of Spironolactone 25 mg tablets because they may contain 50 mg tablets.

    Product
    Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629-1064-02), c) 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1197-2021·2021-03-24

    Medtronic Affinity Pixie Cardiotomy Reservoir Recalled for Bacterial Endotoxin

    Medtronic is recalling 5 units of Affinity Pixie Cardiotomy Reservoirs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION M490817B 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0305-2021·2021-03-24

    Sagent Recalls Phenylephrine Hydrochloride Injection Due to Sterility Concerns

    Sagent Pharmaceuticals is recalling specific lots of Phenylephrine Hydrochloride Injection due to customer complaints of loose vial overseals that may compromise sterility.

    Product
    PHENYLEPHRINE HYDROCHLORIDE — PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1193-2021·2021-03-24

    Medtronic Infant Tubingset Recalled for Elevated Bacterial Endotoxin Levels

    Medtronic is recalling 14 units of infant tubingsets due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack Infant Tubingset Pixie Flow 0,8->1,5-1,8 1/B (PERFUSION M483203D 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V205000·2021-03-24

    Tracker Recalls 2021 Trailers Due to Tire Fender Rubbing

    Tracker Marine is recalling 2021 Ranger Trail and Trailstar trailers because tires may rub against fenders, causing premature wear and increasing the risk of a tire blowout.

    Product
    TRAILSTAR — TRAILSTAR, RANGER TRAIL ZV20, NZ19, NZ21, NZ18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1198-2021·2021-03-24

    Medtronic Pediatric Cardiotomy Reservoir Recalled for Bacterial Endotoxin

    Medtronic is recalling 4 units of a pediatric cardiotomy reservoir due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack CP 1/4-1/4 Pediatric Set 1/B (PERFUSION M484901D 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is…
    Category
    Medical Device
    Distribution
    Distributed nationwide