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. 2,552 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,552 in last 12 months

Showing 1466114680 of 51,038 recalls

DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: 12 HR Allergy & Congestion Relief Fexofenadine HCl Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Relief Allergy Relief D Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Recalled...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 12, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B...

The Issue: Due to a calculation error in the measurement when using 2D trace (manual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...

The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Acclarent, Inc.

Recalled Item: TruDi NAV Suction Instruments: 0-Degree Recalled by Acclarent, Inc. Due to...

The Issue: Suction Instruments were incorrectly calibrated so they may not meet the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 11, 2021· KRAFT HEINZ FOODS COMPANY

Recalled Item: Kool-Aid cherry drink mix powder 19 oz. Recalled by KRAFT HEINZ FOODS...

The Issue: potential for glass and metal in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund