The Recall Desk

State

Vermont product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26451–26475 of 75595

  • SevereFDA (Devices)·Z-1112-2021·2021-02-24

    Combat Medical Systems Recalls Low Titer Type O FWB Transfusion Sets

    Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.

    Product
    Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1110-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Collection Kits

    Combat Medical Systems is recalling 531 Valkyrie LTOWB blood collection kits due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Collection (P/N 80-820, NSN 6515016862423). Blood collection convenience kit. The Valkyrie LTOWB Collection Set includes the items needed to allow for pre-screening to identify Low Titer Type O Donors as well as collect the blood from the donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1111-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Administration Kits

    Combat Medical Systems is recalling 953 Valkyrie LTOWB Administration Sets due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood convenience kit. The Valkyrie LTOWB Administration Set contains the items needed to administer the blood to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V112000·2021-02-24

    2021 International LT Trucks Recalled for Potential Flywheel Detachment

    Certain 2021 International LT vehicles with Cummins X15 engines may have improperly torqued flywheel capscrews that could detach during operation, causing loss of drive power and risk of ejected engine parts.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1109-2021·2021-02-24

    BD 10 ml Syringes Recalled for Potential Open Seals and Sterility Compromise

    Becton Dickinson is recalling 155,200 10 ml syringes because open packaging seals may compromise sterility. The product was distributed in the US and Canada.

    Product
    BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2021·2021-02-24

    Confirm Biosciences Recalls Orient Gene COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Orient Gene COVID-19 Rapid Test Cassettes because they were distributed outside Emergency Use Authorization and not validated for fingerstick use.

    Product
    Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCCOV-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21087·2021-02-24

    Urban Outfitters Recalls Margo Taper Candle Holders Due to Fire Hazard

    Urban Outfitters is recalling Margo Taper Candle Holders because they can catch fire if they contact the flame. One fire incident was reported, with no injuries.

    Product
    Margo Taper Candle Holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2021·2021-02-24

    Getinge CM320 Washer Disinfector Recalled for Hose Deformation Risk

    Getinge is recalling CM320 Series Washer Disinfectors because plastic inlet hose connections may deform or break, potentially causing water leaks and burns.

    Product
    Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing, disinfecting and drying of surgical instruments, containers, operating theatre shoes and operating theatre accessories normally used in hospitals and central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1131-2021·2021-02-24

    Biomet Recalls Mislabelled 25mm Shoulder Prosthesis Central Screws

    Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.

    Product
    Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V110000·2021-02-24

    2021-2022 Polestar 2 vehicles recalled for battery control software glitch

    Polestar is recalling certain 2021-2022 Polestar 2 vehicles. A software issue in the Battery Energy Control Module may cause the high voltage system to disconnect, resulting in loss of drive power and increased crash risk.

    Product
    POLESTAR — POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21086·2021-02-24

    Northern Tool Recalls Powerhorse Generators Due to Electrical Shock Hazard

    Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.

    Product
    Northern Tool & Equipment Powerhorse 13000ES Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1129-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Issue

    GE Healthcare is recalling 96 Revolution CT systems because a damaged or missing table pinch protector may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1130-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Defect

    GE Healthcare is recalling Revolution CT and Revolution CT ES systems because damaged or missing table pinch protectors may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution CT, Revolution CT ES.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21085·2021-02-24

    Potter Electric Recalls Addressable Pull Stations Due to Fire Alarm Failure

    Potter Electric is recalling specific addressable pull stations because the handle may fail to activate the fire alarm, posing a risk of failure to alert occupants to a fire.

    Product
    Potter Electric Addressable Pull Stations Single/Dual Action
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V108000·2021-02-24

    Freightliner Custom XC Chassis Recalled for Missing Brake Return Spring

    Daimler Trucks North America is recalling 2021-2022 Freightliner Custom XC Chassis vehicles because a missing brake pedal return spring may cause brake lights to stay on or brakes to remain engaged.

    Product
    FCCC — FCCC XC CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V111000·2021-02-24

    Audi A8 and S8 Engine Control Module Connector Defect May Cause Engine Stall

    Audi is recalling certain 2019-2021 A8 and 2020-2021 S8 vehicles due to a missing sealing pin on the engine control module connector. Moisture can enter the connector and cause the engine to stall, increasing crash risk.

    Product
    AUDI — AUDI S8, A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1116-2021·2021-02-24

    Medtronic Recalls Cerebrospinal Fluid Valves Due to Radiopaque Marking Issues

    Medtronic Neurosurgery is recalling 22,528 units of STRATA II cerebrospinal fluid valves and shunts worldwide because radiopaque markings may vary in visibility under imaging.

    Product
    Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for the following CFNs: 27739 - SHUNT 27739 STRATA NSC SNAP SML 120CM, 27740 - SHUNT 27740 STRATA NSC SNAP REG 120CM, 27812 - VALVE 27812 STRATA II SM EXTRACTED, 27814 - SHUNT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2021·2021-02-24

    Confirm Biosciences Recalls Healgen COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Healgen COVID-19 Rapid Test Cassettes because they were distributed to non-certified labs and not validated for fingerstick use.

    Product
    Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1128-2021·2021-02-24

    Cairn Diagnostics Recalls 13C-Spirulina Gastric Emptying Breath Test Kits

    Cairn Diagnostics is recalling 103 kits of the 13C-Spirulina Gastric Emptying Breath Test due to a potential for false negative diagnoses of gastroparesis.

    Product
    13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended for use in the measurement of the rate of gastric emptying of solids and as an aid in the diagnosis of delayed gastric emptying (gastroparesis) in adult humans who are symptomatic for gastroparesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2021·2021-02-24

    DLC Laboratories Recalls Sulfur Ointment Jars Due to Labeling Error

    DLC Laboratories is recalling 86,297 jars of Sulfur Ointment 10% because English labels for Camphor were incorrectly applied to the product.

    Product
    Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0264-2021·2021-02-24

    Ascend Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Ascend Laboratories LLC is recalling Cephalexin for Oral Suspension due to CGMP deviations involving unidentified impurities.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide