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. 2,617 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,617 in last 12 months

Showing 1052110540 of 13,380 recalls

DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3))...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 MG/ML Recalled by...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2015· Navinta LLC

Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2015· Hospira Inc.

Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION Recalled by Hospira Inc. Due to...

The Issue: Labeling: Wrong Bar Code: There is a potential for some units to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 5, 2015· Hospira Inc.

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

The Issue: Presence of Particulate Matter: Confirmed finding of human hair floating in...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 5, 2015· Hospira Inc.

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

The Issue: Lack of Assurance of Sterility: there is a potential for solution to leak at...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2015· American Health Packaging

Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· Akorn, Inc.

Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Stability Specifications: Out of specification for preservative,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 25, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...

The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Qualitest Pharmaceuticals

Recalled Item: PROMETHAZINE DM SYRUP (Promethazine Hydrochloride Recalled by Qualitest...

The Issue: Presence of Foriegn Substance: Plastic cap closure particulates may be...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Sagent Pharmaceuticals Inc

Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Sagent Pharmaceuticals Inc

Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...

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

Class II — Potential Health HazardOngoing
Refund