The Recall Desk

State

Vermont product recalls

72,936 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
1,983
Critical
199
Severe
409
Most recent
2026-09-02

Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.

These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2851–2875 of 74919

  • SevereNHTSA·26V146000·2026-03-12

    Honda motorcycle handlebar lock screw may loosen and detach

    Honda is recalling certain 2023-2025 CMX300, CMX500 and CL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.

    Product
    HONDA — HONDA CMX500, CMX300, SCL500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V141000·2026-03-12

    Jeep Wagoneer S liftgate hinge cover may detach from vehicle

    Chrysler is recalling certain 2024-2026 Jeep Wagoneer S vehicles because the liftgate hinge cover may not be properly clipped into position and may detach from the vehicle.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V143000·2026-03-12

    Rolls-Royce Cullinan Recalled for Loose Rear Seat Bolts

    BMW of North America is recalling 2020-2026 Rolls-Royce Cullinan vehicles because loose rear seat bolts may damage seat belts or allow backrests to move.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE CULLINAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26323·2026-03-12

    17 Stories 14-drawer dressers recalled over tip-over and entrapment hazards

    17 Stories Furniture 14-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards. They violate the STURDY Act.

    Product
    17 Stories Furniture 14-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26324·2026-03-12

    Playground swing seat rivets can fail posing a fall hazard

    LFTE USA is recalling Playground Swing Set Seats with model number 999604 because the rivets used to support the swing seat can fail, posing a fall hazard to children.

    Product
    Playground Swing Set Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26319·2026-03-12

    Kluster magnet games recalled because loose magnets pose ingestion hazard

    Kluster Fun Tabletop Magnet Chess Games are being recalled because they contain loose high-powered magnets that fit within CPSC's small parts cylinder, posing an ingestion hazard to children.

    Product
    Kluster Fun Tabletop Magnet Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0388-2026·2026-03-11

    Silintan herbal pills recalled as Class I for undeclared meloxicam

    123Herbals is recalling Silintan 25-count pill bottles because FDA analysis revealed the presence of undeclared meloxicam. The FDA has classified this recall as Class I.

    Product
    SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1471-2026·2026-03-11

    Abiomed Impella RP recalled as Class I over sensor malfunction risk

    Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP. Product Code: 0046-0011.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V140000·2026-03-11

    ATC travel trailer generator exhaust vents under the slide-out bedroom

    Aluminum Trailer Company is recalling certain 2023-2026 PL700 and PL750 recreational trailers because the generator exhaust is vented directly under the slide-out bedroom, letting carbon monoxide enter the cabin.

    Product
    ATC — ATC PL750, PL700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0396-2026·2026-03-11

    Mojo Max Fusion capsules recalled as Class I over undeclared drug ingredients

    Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.

    Product
    Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1470-2026·2026-03-11

    Abiomed Impella RP Flex recalled as Class I over sensor drift

    Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP Flex with SmartAssist. Product Code: 1000323.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1469-2026·2026-03-11

    Abiomed Impella RP with SmartAssist recalled as Class I

    Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP with SmartAssist. Product Code: 0046-0035.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1481-2026·2026-03-11

    B. Braun 21G 4.4 cm winged infusion needles may break

    B. Braun Medical is recalling 21G x 4.4 cm Winged Infusion devices, model 7B3050, because the needle tip may be dull or blunt, difficult to advance, or may break.

    Product
    Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percut
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1491-2026·2026-03-11

    Stago free protein S assay may underestimate normal range results

    Diagnostica Stago is recalling four lots of the STA Liatest Free Protein S kit because of the potential for out-of-range results and underestimation of free protein S in normal patient plasmas.

    Product
    Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0356-2026·2026-03-11

    Teva metoprolol succinate 100 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 100 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0357-2026·2026-03-11

    Teva metoprolol succinate 200 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling three lots of Metoprolol Succinate Extended-Release Tablets 200 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0354-2026·2026-03-11

    Teva metoprolol succinate 25 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 25 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0355-2026·2026-03-11

    Teva metoprolol succinate 50 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1479-2026·2026-03-11

    Olympus lithotripsy generator recalled over transducer recognition failure

    Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris.
    Category
    Medical Device
    Distribution
    Distributed nationwide