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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 28641–28660 of 51,038 recalls
Recalled Item: Toothette Oral Care Suction Swabs with Perox-A-Mint solution. Contains 2...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toothette Oral Care Suction Toothbrushes with Perox-A-Mint solution....
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Q CARE q2 Oral Cleansing & Suctioning System Recalled by Sage Products Inc...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Q CARE q4 Oral Cleaning & Suctioning System Contains 1 Recalled by Sage...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: 5mg strength being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl Injection Recalled by Pfizer Inc. Due to Lack of sterility...
The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levophed (norepinephrine bitartrate) injection Recalled by Pfizer Inc. Due...
The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof-A (Acetaminophen 160 mg Recalled by Centurion Labs, LLC Due to...
The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Recalled...
The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...
The Issue: Olympus has received complaints about fragments of adhesive which detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...
The Issue: Software update to correct several issues that include (1)Potential data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...
The Issue: Intermittent communication between the host system and the FlexCardio
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...
The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...
The Issue: Lack of Assurance of Sterility .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per...
The Issue: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.