Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,603 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,603 in last 12 months

Showing 63016320 of 50,117 recalls

Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.0T Power/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: Evolution Upgrade 3.0T 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: SmartPath to dStream for 1.5T 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 3.0T 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· Philips North America Llc

Recalled Item: MR 5300 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: Ingenia Ambition 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: Intera 1.5T Power/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: Intera 0.5T Standard 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: SmartPath to dStream for XR and 3.0T Recalled by Philips North America Llc...

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 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 T10-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 3.0T Quasar Dual 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: Ingenia 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: Ingenia Ambition 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 Master/Nova 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: Ingenia 3.0T 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· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...

The Issue: Product incorrectly labelled.

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

Class II — Potential Health HazardOngoing
FoodMarch 11, 2024· Canadian Art Prints

Recalled Item: Tranquility & Teachings William Monague plate set Recalled by Canadian Art...

The Issue: Product has been recalled because it may exceed FDA guidance levels for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2024· Advanced Instruments, LLC

Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...

The Issue: System error messages may delay the ability to test patient samples and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Conformis, Inc.

Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...

The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...

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

Class II — Potential Health HazardOngoing