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 46014620 of 28,245 recalls

Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) STERILE TUBE OCCLUDING...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Manual surgical kits labeled as: a) STERILE S/B WIRE SCISSOR...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion STERILE TRACH BRUSH Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Magellan Diagnostics, Inc.

Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...

The Issue: Calibration Buttons being used in the kitting process were incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Bolton Medical Inc.

Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...

The Issue: The stent-graft inside the delivery system was the incorrect size.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Abbott Laboratories

Recalled Item: ARCHITECT STAT Myoglobin Reagent Kit Recalled by Abbott Laboratories Due to...

The Issue: The reason for the recall is the failure of calibration and quality controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Sinus Compress (French) Recalled by Bruder Healthcare Company, LLC...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Back Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Sinus Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing