Ingenia 3.0T, magnetic resonance imaging system.
Philips Medical Systems
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
π₯ Medical Devices β’ 6,554 recalls
Philips Medical Systems
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
Swollen acid bottles due to a trace metal contamination in the Acid Reagent bottles
Philips Medical Systems
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
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.
Philips Medical Systems
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
Potential for the welded seam in affected monitor spring arms to crack and/or break.
Siemens Healthcare Diagnostics
Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate an average upward shift of 24% in QC and patient results following calibration.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Philips Medical Systems
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
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.
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.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.