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. 2,628 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,628 in last 12 months

Showing 66616680 of 28,245 recalls

Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· DeVilbiss Healthcare LLC

Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...

The Issue: The instruction manual is being replaced with an updated version that is in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...

The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Philips North America Llc

Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...

The Issue: If the PM for the telescopic carriage is not performed annually as defined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...

The Issue: If the PM for the telescopic carriage is not performed annually as defined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Radiometer Medical ApS

Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...

The Issue: Due to potential software issue that may result in patient mix-up information.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...

The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· NeuroLogica Corporation

Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...

The Issue: Issue related to the operation of the arm latch within the column that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2023· Compass Health Brands (Corporate Office)

Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....

The Issue: Error in the Introduction section of the user manual that indicates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Philips North America Llc

Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...

The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...

The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...

The Issue: Some batches of product were not sterilized to their minimum sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...

The Issue: Some batches of product were not sterilized to their minimum sterilization...

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

Class II — Potential Health HazardOngoing