Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,624 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,624 in last 12 months

Showing 62816300 of 49,150 recalls

Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0T 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: MR 7700 Recalled by Philips North America Llc Due to Patient support table...

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 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 Achieva 1.5T Pulsar 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: Achieva 3.0TX for PET 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· 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