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. 2,636 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,636 in last 12 months

Showing 63416360 of 51,038 recalls

Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Namic FLUID DELIVERY SET Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic CONVENIENCE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T R11 Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 1.5T Initial Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T S Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN T5-NT Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Achieva Nova Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Achieva IT Nova Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.0T Omni/Stellar Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN ACS-NT Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva XR Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Achieva Nova-Dual Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Ingenia Elition S Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Ingenia Elition X Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Enterprise 1.5T Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing