Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,636 recalls have been distributed to Connecticut in the last 12 months.
Showing 5441–5460 of 28,245 recalls
Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...
The Issue: Potential for damaged and frayed power connector plug with repeated bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...
The Issue: Progressa+ beds have the potential for static buildup from the casters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...
The Issue: Due to product outer packaging incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...
The Issue: Unexpected failure of electrical components within the CPI generator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...
The Issue: Deterioration in the stability of the Test Strips results in diminished...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...
The Issue: Sterilization failures when devices are sterilized per the Reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...
The Issue: There is a potential for unexpected failure of the electrical components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO +VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens .2. Phakic Intraocular lens. Recalled...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.