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. 2,648 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,648 in last 12 months

Showing 39814000 of 51,038 recalls

Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 30, 2024· Deseret Biologicals Inc

Recalled Item: DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules Recalled...

The Issue: Product contains undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2024· Baxter Healthcare Corporation

Recalled Item: Regadenoson Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Labeling: Missing Label

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2024· INCIPIO DEVICES

Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...

The Issue: Recalled lot does not meet specification and has reported incidents of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: La Bonne Vie Camembert 8oz Recalled by SAVENCIA CHEESE USA Due to Potential...

The Issue: potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: Aldi Emporium Selection Brie 8oz Recalled by SAVENCIA CHEESE USA Due to...

The Issue: potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2024· SAVENCIA CHEESE USA

Recalled Item: Glenview Farms Spreadable Brie 2 Recalled by SAVENCIA CHEESE USA Due to...

The Issue: potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Tablet/Capsule Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2024· VIONA PHARMACEUTICALS INC

Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...

The Issue: Due to manufacturing defects observed on Locking Caps that affect the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...

The Issue: Due to manufacturing defects observed on Locking Caps that affect the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2024· Smith & Nephew Inc.

Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....

The Issue: Sterile barrier breach due to inadequate packaging design that could not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Noah Medical

Recalled Item: Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of...

The Issue: Bronchoscopic visualization system power supplies have defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Boston Scientific Corporation

Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...

The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Boston Scientific Corporation

Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...

The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing