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 27061–27080 of 51,038 recalls
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...
The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Molleave Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Conzerol zero molluscum contagiosum Recalled by Elroselabs Inc. Due to cGMP...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Functionality in the report sections "Findings Information" and "Summary of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...
The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...
The Issue: These one-way valves may disconnect at the joint between the two components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.