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. 2,619 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,619 in last 12 months

Showing 98819900 of 51,038 recalls

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
DrugMarch 8, 2023· Pfizer Inc.

Recalled Item: MEKTOVI (binimetinib) tablets Recalled by Pfizer Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle...

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

Class III — Low RiskOngoing
Refund
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
FoodMarch 7, 2023· Natural Solutions Foundation

Recalled Item: Dr. Rima Recommends The Silver Solution Immune System Support Dietary...

The Issue: Product labeled and intended to mitigate, prevent, or treat COVID-19

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

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

Recalled Item: VASOVIEW HEMOPRO 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 3, 2023· Philips North America

Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2023· Philips North America

Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2023· Philips North America

Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2023· Endo Pharmaceuticals, Inc.

Recalled Item: Calcitonin Salmon Nasal Spray Recalled by Endo Pharmaceuticals, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund