State
72,820 recalls have nationwide distribution and so reach Connecticut. 6,564 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,564 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 1,586 (24%) are Severe.
Which agencies issued them
These figures cover only the 6,564 recalls whose distribution notice names Connecticut specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Argon Medical Devices is recalling General Biopsy Tray kits containing Lidocaine HCL Injection because the kits do not meet sterility release criteria.
Abiomed is recalling the Impella 5.5 Smart Assist Set heart pump due to potential leakage from introducer sheaths. The defect is not visually detectable and affects all affected pump sets worldwide.
ABIOMED Impella CP heart pump sets contain introducers that may leak from under the sheath cap and along hub score lines. These manufacturing defects are not visible during use.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nuez Ice Pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40, which pose a serious health risk to consumers with allergies or sensitivities.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Grocella Ice Pop (1 bar, 81.7 g) due to undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.
Olympus Corporation of the Americas is recalling the Olympus Ellik Evacuator (Model 194) worldwide because certain sterilization parameters in the instructions may not render the device adequately sterile.
Chiesi USA, Inc. is recalling Cleviprex (clevidipine) injectable emulsion due to lack of assurance of sterility. The affected product is distributed nationwide.
Olympus is recalling the Toomey Evacuator 50cc with Adaptor (Model 188A) because some sterilization parameters in the instructions may not reliably render the devices sterile.
Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.
Gellert Global Group is recalling Ruby brand Artichoke Hearts Quartered in cans because glass fragments were found in the product. Consumers should not consume affected items.
Medtronic is recalling certain DLP One-Piece Pediatric Arterial Cannulas (Product Number 77010) due to complaints of loose foreign material containing trace levels of blood found in the devices.
GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.
Aluminum Trailer Company is recalling 2026 RM500 and RM700 trailers because the wireless remote may cause unexpected winch movements, increasing injury risk.
Volkswagen is recalling 2024–2026 Atlas and Atlas Cross Sport vehicles due to a low-voltage electrical event that may cause the rearview camera display to fail, reducing rear visibility.
Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.
D'Dioses Tamarindo ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies to these ingredients should not consume the product.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Pina Colada ice pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 dyes.
Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Arroz con Leche Ice Pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 that are not listed on the label.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Mamey Ice Pop (1 Bar, 81.7 g) because it may contain undeclared milk, pecans, pistachios, yellow #5, and red #40.
Coach and Equipment is recalling 2024-2026 Phoenix and Metrolite buses because a wheelchair lift may fail to stop, increasing injury risk.
GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.
Hiab USA Inc. is recalling K-HiPro 425 and 505 cranes because a weld may crack, risking column collapse and injury.
Olympus Corporation is recalling the Glass Body for 194 Ellik Evacuator (Model 190A) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
GE HealthCare recalls certain Optima XR200/220/240amx mobile radiographic systems where safety testing may have been incomplete after column replacement. A failed counterpoise cable could cause the X-ray arm to drop on patients.