Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.
95,018 total recalls in our database
Philips North America
Patient support table floor plate may be incorrectly installed.
SURGICAL SPECIALTIES
Complaints have been received with allegations of Incorrect Needle Curvature.
SonarMed
The failure to detect the partial obstruction in a 2.5mm sensor.
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Philips Respironics
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Philips Respironics
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
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.
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
Philips North America
Patient support table floor plate may be incorrectly installed.