State
73,576 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.
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.
Biomerieux is recalling VIDAS CMV IgM test kits due to reported calibration issues. The recall affects 18,705 kits distributed nationwide and internationally.
Remel Inc is recalling 19 units of Haemophilus Test Medium because lighter-than-normal growth may make antimicrobial test zones difficult to measure.
Boston Scientific is recalling 63 MAMBA Microcatheters due to incorrect labeling and packaging. The devices were distributed nationwide and internationally.
Boston Scientific is removing specific batches of MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.
Centinel Spine is recalling 49 Prodisc C cervical disc prostheses because the 'UP' orientation marking is missing from the superior plate.
Arthrex, Inc. is recalling 32 units of Tibial Opening Wedge Osteotomy Plates because five parts were incorrectly processed as a different model.
Vectornate USA Inc is recalling 130,000 MedSchenker Smart Transport Medium systems due to discoloration and turbidity caused by a longer monsoon season at the manufacturing facility.
Teligent Pharma is recalling Lidocaine Ointment USP, 5%, due to failed viscosity specifications. The recall covers 62,040 tubes distributed nationwide.
Cummins is recalling specific L9 and ISX12 diesel engines because a sealing washer defect may cause fuel leaks, increasing the risk of fire.
Cummins is recalling specific PowerDrive EV electric drivetrains because electromagnetic noise can cause a loss of power steering, increasing crash risk.
Manac is recalling 2018-2019 Steel Platforms, Transfer Trailers, and Square Dump Trailers because steer arm bolts may break, allowing the arm to detach and drag.
Proterra is recalling 2019-2020 Catalyst 40-foot buses because a software defect may allow the rear door to open unexpectedly, increasing injury risk.
TSE Brakes is recalling certain Omni Tandem Brake Chambers because incorrect springs may cause the pressure plate to shift, potentially leading to a loss of air pressure and increased crash risk.
Daimler Trucks North America is recalling Detroit Model 2 and 3 axles because steering arm and tie rod bolts may fracture, potentially causing a loss of steering.
Meritor is recalling specific 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of motive power, increasing crash risk.
Pioneer Coach Interiors is recalling 2019-2020 Prevost H3 and X3 vehicles because a damaged circuit board increases the risk of a fire.
Daimler Trucks North America is recalling 2022 Thomas Built Buses Minotour vehicles because battery cable terminals may contact a fuse block, causing an electrical short circuit and increasing fire risk.
Subaru is recalling 2018-2019 Crosstrek and 2019 Forester vehicles because rear stabilizer bracket bolts may loosen and detach, increasing crash risk.
Tiffin is recalling certain 2021 Phaeton motorhomes with roof-mounted awnings. A roof mounted body panel may be improperly attached and could detach, becoming a road hazard and increasing crash risk.
Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because the engine control module may keep the ignition coil powered after shutdown, causing a short circuit and potential stall.
Simply Delicious Inc. is recalling Bobo's Maple Pecan Oat Bars due to consumer complaints regarding the presence of peanuts.
Alembic Pharmaceuticals is recalling 12,288 bottles of Telmisartan 20 mg tablets due to a label mixup. The product was distributed nationwide in the United States.
Fenwal Inc is recalling specific lots of Amicus MNC Apheresis Kits because centrifuge packs may leak blood during therapeutic procedures.
Becton Dickinson is recalling Martin-Lewis Agar plates because they show heavy fungal growth, which may delay the diagnosis of Neisseria infections.
Arrow International is recalling OnControl Bone Lesion Biopsy Systems because the ejector rod may not insert properly, preventing sample collection.