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Diagnostic Equipment

🏥 Medical Devices 6,627 recalls

The bolt holding the control panel of the ACUSON SC2000 in a fixed position may fail and the Control panel cannot be locked into position.

Jan 12, 2015 Diagnostic Equipment View Details →

This recall has been initiated because use of the impacted DPIs could result in erroneous testing results potentially leading to incorrect diagnosis and incorrect treatment. The magnitude of error for VO2 or VCO2 parameters could be approximately 20% with use of the impacted product.

Dec 23, 2014 Diagnostic Equipment View Details →

Calibration factors in the pump overwritten during a programming step. The force sensor could send a lower signal value to the pump processor, with loss of prime warnings, occlusion alarms and the pump unable to detect a cartridge during the prime sequence. Field action initiated 8/29/2011.

Sep 6, 2011 Diagnostic Equipment View Details →

A required quality control test was not performed during installation associated with the software of the Revolution CT scanner.

Nov 12, 2014 Diagnostic Equipment View Details →

In case of a system crash, images may not be written to the hard disk and this may result in inconsistencies in the database. In case of a system crash (e.g. blue screen, power outage) images may not be written from cache to the hard disk and might get lost.

Jan 13, 2015 Diagnostic Equipment Nationwide View Details →

the Instructions for Use (IFU) were inadvertently removed from the kit.

Dec 16, 2014 Diagnostic Equipment View Details →

Philips has discovered that the Instructions for Use (IFU) for the IntelliVue TcG10 Transcutaneous Gas Measurement Module is missing the contraindication that the device is not to be used on patients under gas anesthesia.

Nov 19, 2014 Diagnostic Equipment View Details →

Potential for composed images to be flipped before being sent to PACS on systems with software version VE10 and SmartOrtho license. Flipped images may be reversed so the associated annotations, e.g. labels (R/L), may be displayed incorrectly, potentially leading to misdiagnosis.

Dec 15, 2014 Diagnostic Equipment View Details →

One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected staining pattern and incorrect patient data.

Dec 19, 2014 Diagnostic Equipment Nationwide View Details →

Device may malfunction, which could cause therapy to be delayed, disabled, or delivered inadvertently.

Nov 19, 2014 Diagnostic Equipment Nationwide View Details →

Three lots of MUM-1 may not meet their labeled shelf life, as a drop in staining intensity over time has been observed.

Dec 12, 2014 Diagnostic Equipment Nationwide View Details →

Software Anomaly: the firm has identified an anomaly with VITROS System Software Version 3.1 and below, and determined that the software may not properly identify an expired calibration.

Nov 19, 2014 Diagnostic Equipment Nationwide View Details →

Software Anomaly: the firm has identified an anomaly with VITROS System Software Version 3.1 and below, and determined that the software may not properly identify an expired calibration.

Nov 19, 2014 Diagnostic Equipment Nationwide View Details →