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

51,038 total recalls
939 in last 12 months

Showing 44661–44680 of 51,038 recalls

FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Pecan Bueno Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043W-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1777: Umbilical (2) 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1762: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4040-2: Umbilical 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...

The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...

The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...

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

Class III — Low RiskOngoing
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: Dollar General Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: Dr. Sheffield Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: FAMILY wellness Triple Antibiotic Ointment. NET WT 1 OZ (28 g) Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2013· B. Braun Medical Inc

Recalled Item: Cefepime for Injections USP and Dextrose Injection USP Recalled by B. Braun...

The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...

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

Class I — Serious Health HazardOngoing
Refund