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.

51,038 total recalls
2,445 in last 12 months

Showing 2996129980 of 51,038 recalls

DrugMay 16, 2017· Lupin Limited (Unit 1)

Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...

The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 15, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...

The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Beckman Coulter Inc

Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...

The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...

The Issue: Potential for electric shock in the case of a failure to install the...

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

Class II — Potential Health HazardOngoing
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Tofu in Polybag 40/240g Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Ball in Polybag 24/12oz. Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 20/1lb. Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 10/930g Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 10/2.2lbs Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 12, 2017· Italian Gluten Free Foods CL

Recalled Item: Chef Luca's Italian Gluten Free Foods Lasagna Al Forno Baked Cheese Lasagna...

The Issue: Product contains undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 12, 2017· Mesa Laboratories, Inc.

Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....

The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Teleflex Medical

Recalled Item: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets...

The Issue: Product size listed on the labeling is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-107 Recalled by Becton Dickinson & Co. Due to BD has...

The Issue: BD has recently confirmed quality control failures, related to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...

The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing