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. 939 recalls have been distributed to Connecticut in the last 12 months.
Showing 47821–47840 of 51,038 recalls
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened..
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened..
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...
The Issue: Chemical contamination: emission of strong odor after package was opened.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Obturator Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helistat Absorbable Hemostatic Recalled by Integra LifeSciences Corporation...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...
The Issue: The problem is that the "static tolerances" from the calibration files...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...
The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...
The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.