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Diagnostic Equipment

πŸ₯ Medical Devices β€’ 6,627 recalls

The MRx monitor/defibrillators could fail to charge because the therapy printed circuit board may have been loaded with an incorrect electronic component. Failure to charge could potentially cause therapy to be interrupted or delayed.

May 3, 2018 Diagnostic Equipment View Details β†’

Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised.

May 11, 2018 Diagnostic Equipment View Details β†’

Possibility that the Biograph Horizon systems performing CT retrospective cardiac gating or PET cardiac gating examinations may experience a waveform sampling issue caused by a firmware change within the Universal Physiological Measurement Module.

Feb 21, 2018 Diagnostic Equipment View Details β†’

The Strip Provider Modules (SPM) on some of the instruments had not been inspected during manufacture for correct seal placement and integrity.

Mar 29, 2018 Diagnostic Equipment View Details β†’

Software anomaly resulting in the loss of patient settings and stored patient data.

Mar 28, 2018 Diagnostic Equipment Nationwide View Details β†’

The real-time numeric value for ventricular end-diastolic pressure (EDP) displayed on the Live Display may be inaccurate. Because ventricular pressure monitoring is only performed in the cardiac catheterization procedure room using the FC2010 device, the FC2020 device, which is used in the Pre or Post-Op Holding Areas, is not impacted by this issue.

Mar 14, 2018 Diagnostic Equipment Nationwide View Details β†’

A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has an incorrect pad placed in the location of the leukocytes pad. This will result in control CB failure for leukocytes and may generate false negative erroneous results for leukocytes.

Dec 4, 2017 Diagnostic Equipment Nationwide View Details β†’

A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.

Apr 5, 2018 Diagnostic Equipment View Details β†’

The assay can potentially generate erroneously elevated or erroneously decreased HbA1c patient results.

Mar 5, 2018 Diagnostic Equipment Nationwide View Details β†’

A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.

Apr 5, 2018 Diagnostic Equipment View Details β†’

A failure of the tube arm suspension is possible while the tube arm height is being adjusted. During tube height adjustment there is a small probability of failure of both the primary and redundant holding mechanisms, causing uncontrollable descent of the tube arm and a potential risk of injury to the patient.

Apr 5, 2018 Diagnostic Equipment View Details β†’

The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.

Apr 27, 2017 Diagnostic Equipment Nationwide View Details β†’