The Recall Desk

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.

23426–23450 of 75512

  • SevereFDA (Food)·F-0169-2022·2021-11-17

    Bobo's Almond Butter Protein Bars recalled for undeclared peanuts

    Simply Delicious, Inc. is recalling Bobo's Almond Butter Protein Bars (2.2 oz.) because they contain undeclared peanuts, posing a risk to consumers with peanut allergies.

    Product
    Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves. UPC 8-29262-00201-6 (Individual bar) UPC 8-29262-00326-6 (4-Pack Multipack) UPC 8-29262-00370-9 (Master Case of 6 sleeves) Storage ambient.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V893000·2021-11-17

    Motorhome seat belt retractor defect affects child restraint systems

    Jayco recalls certain 2021-2022 motorhomes with defective seat belt retractors that may fail to secure child restraint systems during crashes. Dealers will replace the retractors free of charge.

    Product
    JAYCO — JAYCO, ENTEGRA SWIFT, ETHOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0208-2022·2021-11-17

    Safety Blood Collection Needle Recalled for Safety Mechanism Activation Issues

    Zhejiang Kindly Medical Devices is recalling Henry Schein Safety Blood Collection Needles due to potential difficulty activating the safety mechanism. Affected lot numbers distributed nationwide.

    Product
    HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch, REF 570-2067, 100pcs/box 1000pcs/ctn 350*210*350mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V896000·2021-11-17

    Freightliner and Western Star trucks recalled for unapproved tires and wheels

    Daimler Trucks North America is recalling Freightliner 108SD, 114SD, Coronado, and Western Star trucks from model years 2012-2022 due to unapproved tires and rims that do not meet federal safety standards.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, 4900, 4700, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2022·2021-11-17

    McKesson PREVENT HT Winged Blood Collection Needles Recall for Safety Mechanism Difficulty

    McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.

    Product
    McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH21GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0211-2022·2021-11-17

    QuikClot Combat Gauze Recalled for Potential Sterile Packaging Seal Failure

    Z-Medica is recalling 2400 units of QuikClot Combat Gauze due to potential packaging seal failures that could compromise sterile barrier integrity. Affected lot 12645 was distributed nationwide.

    Product
    QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0213-2022·2021-11-17

    Philips Azurion X-Ray Systems may lock up during simultaneous button presses

    Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.

    Product
    Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0205-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled Over Safety Mechanism Activation Risk

    Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled for Safety Mechanism Defect

    McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 21G 1 1/4 inch, MFR # 16-NBC21GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V889000·2021-11-17

    Toyota Recalls 2022 Sienna Models Due to Seat Belt Webbing Guide Defect

    Toyota is recalling 2022 Sienna and Sienna Hybrid vehicles with eight-passenger seating because an incorrect seat belt webbing guide may cause the belt to tear during a crash.

    Product
    TOYOTA — TOYOTA SIENNA HYBRID, redundant SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0206-2022·2021-11-17

    McKesson PREVENT HT Blood Collection Needle Safety Mechanism Activation Issue

    McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.

    Product
    McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0215-2022·2021-11-17

    Hemodialysis Delivery System Software May Use Incorrect Treatment Parameters

    Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.

    Product
    Hemodialysis Delivery System, Software Version 2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2022·2021-11-17

    Safety Blood Collection Needles Recalled Due to Safety Mechanism Activation Difficulty

    Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.

    Product
    HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2022·2021-11-17

    Tadalafil Tablets Recalled Due to Incorrect Product Formulation

    Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0156-2022·2021-11-17

    NOW Ginseng & Royal Jelly supplement may contain Metronidazole

    NOW Health Group Inc. is recalling NOW Ginseng & Royal Jelly 90 VCAPS and MMA Nutrition Ginselin 90 Veg Capsules because the products may contain Metronidazole, an undeclared pharmaceutical ingredient.

    Product
    NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Veg Capsules UPC 733739440075
    Category
    Drug
    Distribution
    47 states
  • ModerateFDA (Food)·F-0155-2022·2021-11-17

    NOW Royal Jelly supplements may contain undeclared Metronidazole

    NOW Health Group Inc. is recalling NOW Royal Jelly 1500mg capsules and related private label versions because they may contain Metronidazole, an undeclared pharmaceutical ingredient. The recall affects approximately 88,890 units distributed across the United States and internationally.

    Product
    NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC 733739150523 Lifesource Vitamins 1500mg 60 Veg Caps UPC 610265580430
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0157-2022·2021-11-17

    NOW Bee Pollen 500mg Capsules Recalled for Metronidazole Contamination

    NOW Health Group Inc. is recalling NOW Bee Pollen 500mg 100 VCAPS (UPC 733739025203) because the product may contain Metronidazole, an antibiotic not listed on the label.

    Product
    NOW Bee Pollen 500mg 100 VCAPS UPC 733739025203
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Drugs)·D-0230-2022·2021-11-17

    Tadalafil Tablets Recalled for Incorrect Product Formulation

    Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0095-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling Acetaminophen Oral Suspension (325 mg/10.15 mL) due to contaminated raw ingredient used in manufacturing. The recall affects 151,100 unit dose cups distributed nationwide for hospital use.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0094-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling 166,920 unit dose cups of Acetaminophen Oral Suspension 160 mg/5 mL (Lot 503670) distributed nationwide due to cGMP deviations involving contaminated raw ingredient used in manufacturing.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V886000·2021-11-16

    Jayco Recalls 2020-2022 Motorhomes Due to Rear Suspension Fastener Defect

    Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA, ANTHEM, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V885000·2021-11-16

    2021 Entegra Cornerstone Motorhome Power Steering Pump Defect Recall

    Jayco recalls certain 2021 Entegra Cornerstone motorhomes with a power steering pump defect that may result in loss of steering assist. Owners should contact Jayco for free pump replacement to prevent increased crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V887000·2021-11-16

    EBY Generation Trailers Recalled for Missing Rear Conspicuity Tape

    M H Eby is recalling 2020-2022 EBY Generation trailers because missing white conspicuity tape on the top rear corners reduces visibility to other drivers.

    Product
    EBY — EBY GENERATION
    Category
    Vehicle
    Distribution
    Distributed nationwide