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. 2,664 recalls have been distributed to Connecticut in the last 12 months.
Showing 2981–3000 of 51,038 recalls
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...
The Issue: In situations where two images with differing Fields of View (FOV) complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...
The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glicks Dark Chocolate Conettos Recalled by Kenover Marketing Corp. Due to...
The Issue: Undeclared Allergen (Milk)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.