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. 2,456 recalls have been distributed to Connecticut in the last 12 months.
Showing 22741–22760 of 28,245 recalls
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Trifurcated Ext set Recalled by Churchill Medical Systems, Inc....
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgical System Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The Wall chart has been updated because it was noted that Wall Chart (PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storm Series Electric Wheelchair. Invacare FDX Recalled by Invacare...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely-depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...
The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.