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. 1,032 recalls have been distributed to Connecticut in the last 12 months.
Showing 20661–20680 of 51,038 recalls
Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...
The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...
The Issue: The boxes used by the shipper were not validated for use during transport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickDraw Venous Cannula Recalled by Edwards Lifesciences, LLC Due to If the...
The Issue: If the venous cannula is used in an unintended manner (longer than 6 hours;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals, LLC Due to Foreign...
The Issue: Presence of Foreign Substance: Foreign material found inside the vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iMRX MRI and Angiography System Recalled by Deerfield Imaging, Inc. Due to...
The Issue: There is a potential hardware error for the iMRX System with a generator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...
The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...
The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...
The Issue: During a routine inspection of a system, a crack on the C-arm holder was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...
The Issue: Cross contamination with other products: undeclared contaminants of phenol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Discoloration: Product complaints of discoloration after reconstitution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....
The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Recalled by...
The Issue: The abutment provided with the Implant System may be out of specification,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.