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.
Target is recalling Cat & Jack Baby Heart Ears Rompers because heart-shaped graphics on the knees can detach, posing a choking hazard to children.
Playgro is recalling Clip Clop infant activity rattle toys because the abacus ring can dislodge and release small beads, posing a choking hazard to small children.
Fenwal Inc is recalling 2,466 Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.
Battat is recalling B. toys Firefly Frank infant teethers sold at Target because plastic wings can detach, posing a choking hazard to young children.
ROi CPS LLC is recalling 16 Regard custom cardiovascular procedure kits because drape slits may breach the sterile barrier.
Fenwal Inc is recalling 24 units of Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.
Siemens is recalling 12 Ysio X.pree digital X-ray systems because a software issue may display a previous patient's image during recovery, potentially impacting diagnosis.
Audio-Technica is recalling charging cases for ATH-CK3TW wireless headphones because they can overheat and pose a fire hazard. No injuries have been reported.
Becton Dickinson is recalling BD BBL Martin-Lewis Agar due to misformulation causing heavy fungal growth, which may delay the diagnosis of Neisseria infections.
Hologic is recalling 1,355 Panther Fusion Tube Trays because they may leak, potentially causing false positive, false negative, or invalid patient results.
Fujifilm Medical Systems is recalling Synapse PACS software because it may display incorrect patient information in the viewer or PowerJacket.
Medtronic is recalling A610 Clinician Programmer software versions 2.0.4584, 2.0.4594, 2.0.4605, and 3.0.1057 due to software errors that prevent proper copying of cycling settings and cause application crashes when reading full system event logs.
Terumo is recalling 12 sternal retractor devices because the stainless steel locking plates may fracture. The devices were distributed in eight US states.
Apotex Corp. is recalling Guanfacine Extended-Release tablets because they contain trace amounts of Quetiapine Fumarate.
Cosette Pharmaceuticals is recalling specific lots of Mometasone Furoate Topical Solution due to Current Good Manufacturing Practice (CGMP) deviations.
Gf Health Products is recalling 66 units of the Drop Arm Versamode because the front casters are incorrect. The devices were distributed in the US and internationally.
Nuvasive Specialized Orthopedics is recalling PRECICE limb lengthening devices because they lack full biological assessments and are not indicated for patients under 18.
Nuvasive Specialized Orthopedics Inc. is recalling 59 units of Freedom End Caps and related components because they lack full biological assessments and are not indicated for patients under 18.
X-Gen Pharmaceuticals is recalling Neomycin Sulfate Tablets 500mg because a microbiological assay failed to meet stability specifications.
Clerio Vision is recalling 153 Extreme H2O 59% contact lenses because they may be mislabeled with the incorrect lens power.
New Generation Wellness Inc. is recalling 2,330 bottles of Vegan Vitamin D3 tablets because stability samples showed potency below the label claim.
Kimberly-Clark is recalling Scott Moisturizing Foam Hand Sanitizer because some bottles containing Foam Skin Cleanser soap are incorrectly labeled as hand sanitizer.
Nuvasive Specialized Orthopedics is recalling Precice Unyte orthopedic trauma nails because they lack full biological assessments and are not indicated for patients under 18.
Sun Pharmaceutical Industries is recalling 2,520 bottles of Metformin Hydrochloride Extended-Release Tablets due to failed moisture limits.
New Generation Wellness Inc. is recalling Live Better vegan vitamin D-3 tablets because stability samples showed less than 100% of the label claim.