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. 2,442 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,442 in last 12 months

Showing 3220132220 of 51,038 recalls

Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige SI Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: RFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCV+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestilix Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Innova 2000 Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Legacy Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCLP+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCN+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: SFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Oculus Innovative Sciences, Inc.

Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...

The Issue: Firm became aware that professional samples of Ceramax are not meeting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2016· Shimadzu Medical Systems

Recalled Item: Shimadzu X-ray TV System Recalled by Shimadzu Medical Systems Due to...

The Issue: Shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION...

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

Class II — Potential Health HazardOngoing
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Lidocaine HCl 1% Recalled by Cantrell Drug Company Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Oxytocin 30 USP Units Added to 0.9% Sodium Chloride Recalled by Cantrell...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Calcium Chloride Recalled by Cantrell Drug Company Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 2 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Heparin Sodium Recalled by Cantrell Drug Company Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Fentanyl Citrate 1 Recalled by Cantrell Drug Company Due to Lack of...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

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

Class II — Potential Health HazardOngoing
Refund