Recalls affecting Connecticut
Notices that name Connecticut in their distribution area, plus every nationwide recall — nationwide recalls reach Connecticut too.
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NHTSA safety recall · last month
Chrysler recall: Due to a software error, the tire pressure monitoring system may fail
Due to a software error, the tire pressure monitoring system may fail to detect low tire pressure and/or fail to illuminate the tire pressure…
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NHTSA safety recall · last month
Chrysler Voyager and Chrysler Pacifica recall: The brake pedal position sensor capacitor may be cracked
The brake pedal position sensor capacitor may be cracked, which can cause a loss of electronic stability control. As such, these vehicles fail to…
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Highest risk · 2 months ago
Walmart Reannounces of Mainstays Nine-Drawer Fabric Dressers recall: Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards
Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through…
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Highest risk · 2 months ago
Haba USA Rainbow Rattle Grasping and Teething Toys recall: Risk of Serious Injury or Death from Choking and Ingestion Hazards
Risk of Serious Injury or Death from Choking and Ingestion Hazards
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Highest risk · 2 months ago
Excel Industries Accessory LED Light Kits recall: Risk of Serious Injury from Fire Hazard
Risk of Serious Injury from Fire Hazard
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Highest risk · 2 months ago
AudioLineOut Studio Six Headphone Amplifiers recall: Risk of Serious Injury or Death from Electrocution Hazard
Risk of Serious Injury or Death from Electrocution Hazard
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Class II · 2 months ago
SDI Limited Dentsply Sirona Capsule Mixer recall: Potential for electrical discharge from unit when unplugged
Potential for electrical discharge from unit when unplugged.
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Class II · 2 months ago
Maquet Critical Care AB Getinge Y Sensor Module, Servo-U, Servo-N recall: The module did not undergo electrical safety tests and functional tests
The module did not undergo electrical safety tests and functional tests during production.
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Class II · 2 months ago
Arrowhead DE LLC Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525 recall: Implant did not undergo required gamma radiation dose audit. A potential
Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
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Class II · 2 months ago
Tobii Dynavox Llc TD Navio Maxi Speech Generating Device Model/ recall: Under certain conditions, the battery mounting tabs may become damaged
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading…
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Class II · 2 months ago
Beckman Coulter DxC 500i Clinical Analyzer Modules using software recall: a software defect in which the Parameter Package (PP) import logic overwrites
a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously…
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Class II · 2 months ago
Gentherm Medical, LLC Innercool Coolblue Console, Model STx recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
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Class II · 2 months ago
Fort Defiance Industries recall: The Automated Field Steam Sterilizer's water recovery system 120V Amphenol
The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which…
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Class II · 2 months ago
Gentherm Medical, LLC Blanketrol III, Model 233 recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
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Class I · 2 months ago
Boston Scientific Enroute Transcarotid Neuroprotection System recall: Potential for arterial sheath tip separation or partial tip separation during
Potential for arterial sheath tip separation or partial tip separation during use.
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Class II · 2 months ago
Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software recall: a software defect in which the Parameter Package (PP) import logic overwrites
a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously…
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Class I · 2 months ago
Boston Scientific Enroute Transcarotid Neuroprotection System Plus recall: Potential for arterial sheath tip separation or partial tip separation during
Potential for arterial sheath tip separation or partial tip separation during use.
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class II · 2 months ago
Siemens Healthineers Immulite 2000 Systems SYP recall: Syphilis Screen assay may contain a negative patient bias resulting in low
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
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Class II · 2 months ago
ConvaTec, Inc Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703 recall: Urostomy Pouches may leak from cap during use
Urostomy Pouches may leak from cap during use.
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Class II · 2 months ago
Philips North America Llc Cardiac Workstation 7000. Product Number: 860441 recall: Device will intermittently provide inaccurate data related to native heart
Device will intermittently provide inaccurate data related to native heart rate.
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Class II · 2 months ago
Covidien, LLC EndoFlip System that includes: Endoflip 1 System EF-100 05391530810050 recall: The system's 24-hour usage limit results in catheters incorrectly flagged
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Small Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class II · 2 months ago
Boston Scientific Corporation Suture Cinch Long 1pk. Endoscopic tissue approximation recall: Device may fail to deploy the cinch implant and/or fail to cut the suture
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.