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. 1,079 recalls have been distributed to Connecticut in the last 12 months.
Showing 14201–14220 of 28,245 recalls
Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...
The Issue: Compromised seal on the sterile barrier pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...
The Issue: There may be dimensional manufacturing error that represents a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...
The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...
The Issue: New software version for affected ventilators reduces the probability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.