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 53015320 of 28,245 recalls

Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE PVP SLN KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PVP SOLUTION SING STRL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· Liberty Medical Solutions, LLC

Recalled Item: Multi-Mode Stimulator Recalled by Liberty Medical Solutions, LLC Due to The...

The Issue: The instruction manuals that were included with the Multi-Mode Stimulators...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...

The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· B. Braun Medical, Inc.

Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...

The Issue: In affected products, the tubing outer diameter may vary in size or the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...

The Issue: Under certain circumstances, information from HL7 messages received by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software issue where "low" and "terminal" battery alerts did not display...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Positioner Arm may not tighten or lock during normal use.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· KENT IMAGING, INC.

Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...

The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...

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

Class II — Potential Health HazardOngoing