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 29801–29820 of 51,038 recalls
Recalled Item: Tissu-Trans Filtron 500 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...
The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...
The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...
The Issue: Hub damage resulting in breakage and/or leakage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...
The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Whole Foods Cranberry Couscous- packaged in Clear plastic clamshell for 6oz...
The Issue: Product contains undeclared tree nuts-cashews
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...
The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...
The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...
The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...
The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...
The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.