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. 2,643 recalls have been distributed to Connecticut in the last 12 months.
Showing 5241–5260 of 28,245 recalls
Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...
The Issue: Due to incorrect product/device within packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT Recalled by Smiths Medical Asd...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex LOGICAL CATH LAB KIT Recalled by Smiths Medical Asd Inc Due to There...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux 2006/ 2007 Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/...
The Issue: The internal diameter of the coaxial cannula may be smaller or larger than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED/HLED and PowerLED300 OR Light Systems Recalled by Getinge...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Blueline Series 30/80 OR Light Systems Recalled by Getinge Usa Sales...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Rolite OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Lucea - Lucea10/40 Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLEDII OR Light System Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Equipment OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Volista Recalled by Getinge Usa Sales Inc Due to A potential for a...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux HLX3000 OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet G8 / G8E OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.