State
72,936 recalls have nationwide distribution and so reach Connecticut. 6,566 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,566 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,588 (24%) are Severe.
Which agencies issued them
These figures cover only the 6,566 recalls whose distribution notice names Connecticut specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 588 units of the HOT AXIOS Stent and Electrocautery-Enhanced Delivery System, 20mm x 10mm after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 150 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 8mm x 8mm, after increased reports of stent deployment and expansion issues.
B.C. Williams Bakery Service is recalling 51 bags of Spice Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
B.C. Williams Bakery Service is recalling 95 bags of Swiss Chocolate Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
Boston Scientific is recalling 557 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 20mm x 10mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 266 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
B.C. Williams Bakery Service is recalling 720 bags of Bread and Roll Mix, sold in 50 lb bags, over an undeclared milk allergen.
Boston Scientific is recalling 59 units of the AXIOS Stent and Electrocautery-Enhanced Delivery System, 8mm x 8mm after increased reports of stent deployment and expansion issues.
Nissan is recalling certain 2024-2025 Rogue vehicles with the 1.5L VC-Turbo engine because the gears in the electronic throttle body assembly may break, causing a loss of drive power.
General Rubber is recalling specific Xcellent Roadbreaker A/T tires that may crack and separate, increasing the risk of a crash.
Nissan is recalling certain 2023-2025 Rogue vehicles with the 1.5L VC-Turbo engine because increased temperatures can break down the engine oil, causing the bearings to seize and the engine to fail.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Olympus is recalling 3,361 Single Use Electrosurgical Knife KD-645 units because deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Olympus is recalling the Single Use Electrosurgical Knife KD-640L because deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Changchun Wancheng Bio-Electron is recalling 91,366 units of LotFancy Urinary Tract Infection Urine (UTI) Test Strips because tests requiring a 510(k) were distributed before they could be legally marketed.
Triumph is recalling certain 2022-2024 Bonneville, Street Twin, Street Scrambler, Speed Twin 900 and Scrambler 900 motorcycles because the wiring between the alternator and main harness connector may short circuit.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Tornier is recalling 427 Perform Reversed peripheral screws because a lot labeled 5.0mm x 18mm actually contains 5.00mm x 14mm screws.
Changchun Wancheng Bio-Electron is recalling 1,000 units of the S. Typhi/Para Typhi A Antigen test because it was distributed before it could be legally marketed.
Diva Fam is recalling Sea Moss Gel Superfood in the Cherry variety over potential Clostridium botulinum contamination.
Changchun Wancheng Bio-Electron is recalling 32,500 units covering The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips because tests requiring a 510(k) were distributed before they could be legally marketed.
Diva Fam is recalling Sea Moss Gel Superfood in the Blue Spirulina and Raspberry variety over potential Clostridium botulinum contamination.
Changchun Wancheng Bio-Electron is recalling 3,300 units of Vivoo Sodium Test because tests requiring a 510(k) were distributed before they could be legally marketed.
Fujirebio Diagnostics is recalling 128 units of Lumipulse G beta-Amyloid 1-42-N Plasma Calibrators because falsely elevated ratio results can incorrectly classify a patient as having amyloid pathology.