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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 27081–27100 of 51,038 recalls
Recalled Item: Lupin Cefdinir powder for Oral Suspension USP Recalled by Lupin...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.54% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.75% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Signature Care Calcium Chews Recalled by Bestco, Inc. Due to A packaging...
The Issue: A packaging revision and lack of revision to the corresponding packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MMRF Ela Ada Jaggery Recalled by Maharaja Food Importers, Inc. Due to Label...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELA ADA (JACK FRUIT) Recalled by Maharaja Food Importers, Inc. Due to Label...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MMRF Kumbiliappam Recalled by Maharaja Food Importers, Inc. Due to Label...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Parotta Family Pack Recalled by Maharaja Food Importers, Inc. Due to Label...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WHOLE WHEAT PAROTTA Recalled by Maharaja Food Importers, Inc. Due to Label...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MMRF Neyyappam Recalled by Maharaja Food Importers, Inc. Due to Label states...
The Issue: Label states ghee, but does not declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.