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. 914 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
914 in last 12 months

Showing 50441–50460 of 51,038 recalls

FoodMay 4, 2012· FunFresh Foods Inc

Recalled Item: FunFresh Foods World Berry Organic Cacao Nibs 6 oz Recalled by FunFresh...

The Issue: FunFresh Foods World Berry Cacao Nibs 6 oz snack food contaminated with E. coli.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 6IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Scenaria CT System Software Product Usage: The Scenaria system...

The Issue: Hitachi discovered a software error in the Reconstruction Status function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 4IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 20% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2012· Arrow International Inc

Recalled Item: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)...

The Issue: Lidstock of product does not contain chlorhexidine contraindication and...

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

Class I — Serious Health HazardOngoing
DrugMay 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Zeosa (norethindrone and ethinyl estradiol tablets USP Recalled by Teva...

The Issue: Impurities/Degradation: This recall is being carried out due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Midazolam HCl Injection Recalled by Ben Venue Laboratories Inc Due to Short...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Octreotide Acetate Injection Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 525 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing