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. 2,643 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,643 in last 12 months

Showing 46414660 of 28,245 recalls

Medical DeviceFebruary 19, 2024· Thoratec Corp.

Recalled Item: HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Recalled...

The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2024· ConvaTec, Inc

Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...

The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Ten 10ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· CooperSurgical, Inc.

Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...

The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Medtronic Inc.

Recalled Item: Abre Venous Self-expanding Stent System Recalled by Medtronic Inc. Due to...

The Issue: There is a potential for sterile package breach.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Biosense Webster, Inc.

Recalled Item: CARTO VIZIGO Bi-Directional Guiding Sheath Recalled by Biosense Webster,...

The Issue: Due to a manufacturing issue, device under process validation phase were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2024· Medivance Inc.

Recalled Item: Medivance Neonatal ArcticGel Pads Recalled by Medivance Inc. Due to Neonatal...

The Issue: Neonatal pads are experiencing reduced water flow, which may reduce or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Bio-Rad Laboratories

Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...

The Issue: Due to incorrect calibrations and controls, their is a potential of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Mariner RDX Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION Due...

The Issue: Screw heads, of pedicle screw systems, have thin lead-in thread that pose a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Philips North America Llc

Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...

The Issue: If the DIVA touch display generates touch inputs without user interaction,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Covidien, LP

Recalled Item: Signia" Small Diameter Curved Tip Intelligent Reload Recalled by Covidien,...

The Issue: Under certain firing conditions, reloads were found to articulate in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload Recalled by...

The Issue: Under certain firing conditions, reloads were found to articulate in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Randox Laboratories Ltd.

Recalled Item: Cystatin C Calibrator - In vitro diagnostic (IVD) use in Recalled by Randox...

The Issue: Cystatin C Calibrator Series CVS 2699, is running with a negative bias...

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

Class II — Potential Health HazardOngoing