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 5081–5100 of 51,038 recalls
Recalled Item: Umary Acido Hialuronico Recalled by SoloVital Due to Undeclared Diclofenac
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7100 Recalled by Datex-Ohmeda, Inc. Due to Potential issue that may...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...
The Issue: There is a potential that the robotic system's instrument cart arm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RMU-2000 Automated Chest Compression Device Recalled by Defibtech, LLC Due...
The Issue: Problem in the device's motor may cause the device to stop compressions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wiers Farm - Hungarian Wax Peppers packaged into 1lb carton Recalled by...
The Issue: Listeria monocyotgenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wiers Farm - Cilantro packaged into 1lb cartons - 30 Recalled by Wiers Farm...
The Issue: Listeria monocyotgenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wiers Farm - Organic Bell Peppers packaged into 2 count Recalled by Wiers...
The Issue: Listeria monocyotgenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.