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. 1,739 recalls have been distributed to Connecticut in the last 12 months.
Showing 47581–47600 of 51,038 recalls
Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Form Amino Acids L-Arginine 7 L-Ornithine Complex With Alpha-Lipoic...
The Issue: Nexgen Pharma is recalling a certain lot of dietary supplement L-Arginine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sermorelin/GHRP-6 Recalled by NuVision Pharmacy, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The firm is recalling all lots of sterile products compounded Recalled by...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG (Lyophilized) Stock # 21714 Recalled by NuVision Pharmacy, Inc. Due to...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentrexcilina (acetaminophen Recalled by OPMX, LLC Due to Labeling: Not...
The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentrexcilina Jarabe NF (dextromethorphan HBr and guaifenesin) liquid...
The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Staple Remover Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various types of Fetal Bovine Serum Bovine sourced Animal Sera Recalled by...
The Issue: Current product labeling band data sheets state that FBS Pharma Grade and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.