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Diagnostic Equipment

πŸ₯ Medical Devices β€’ 6,554 recalls

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

BioFire has identified an increased risk of false positive results when the FilmArray Blood Culture Identification (BCID) Panel is used with bioMΒΏrieux BacT/ALERT Standard Anaerobic (SN) blood culture bottles. False positive results have been observed for Pseudomonas aeruginosa and Enterococcus.

May 27, 2014 Diagnostic Equipment Nationwide View Details β†’

Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate an average upward shift of 24% in QC and patient results following calibration.

Sep 17, 2013 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman Coulter Access Family of Immunoassay Systems because the bottle labeled as Calibrator Level 5 actually contains Calibrator Level 4. This results in a calibration failure when attempting to calibrate using a calibrator kit which contains the affected Level 5 Calibrator.

May 30, 2014 Diagnostic Equipment Nationwide View Details β†’

Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to a potential chance of losing network connection after switching from hardwired Ethernet connection to using the Qube Docking Station without powering down the device. The bedside monitor and all of its alarms will continue to function normally. No one has been injured as a result of this issue.

Jun 6, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’

Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.

May 28, 2014 Diagnostic Equipment Nationwide View Details β†’