April 24, 2024Medical DevicesFDA
Conformis, Inc. recalls Identity Imprint PS Tibial Tray Size 4: Lot 540287
Hazard: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot 540287. It was confirmed that Lot 540287 and Lot 508287 were swapped between the pouching and final pack.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls SmartPath to dStream for 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls MR 7700, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls MR 5300, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera CV, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 3.0T Quasar Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T R11, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Power/Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Omni/Stellar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Master/Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T Achieva IT Nova, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.0T Power/Pulsar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 1.0T Omni/Stellar, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Intera 0.5T Standard, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Elition X, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Elition S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Ambition X, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia Ambition S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 3.0T CX, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 3.0T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T S, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T CX, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls Ingenia 1.5T, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.
April 24, 2024Medical DevicesFDA
Philips North America Llc recalls GYROSCAN T5-NT, Magnetic Resonance System.
Hazard: Patient support table floor plate may be incorrectly installed.