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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

Flowonix Medical received a report of a patient implanted with the Prometra II Programmable Pump who may have received a fatal drug overdose during an MRI procedure. The Prometra II pump has an FDA-approved design feature intended to permit safe exposure to an MRI without removing drug from the reservoir.

May 22, 2017 Implants & Prosthetics Nationwide View Details β†’

A customer reported that when using an NX workstation with software version NX 3.0.8950 software and selecting the affected patient/exam from closed exams, initially the wrong image was linked to the exam and appeared. After a short time the wrong image was replaced by the correct image, however the wrong image was used for transmitting to PACS.

Dec 21, 2016 Diagnostic Equipment Nationwide View Details β†’

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Apr 13, 2017 Other Medical Devices Nationwide View Details β†’

Failures can result due to a component defect on Artis zee systems with an A100 Plus generator of a certain delivery lot and 2-focus Megalix Cat Plus tube unit.

Feb 3, 2017 Diagnostic Equipment View Details β†’

BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.

Sep 16, 2016 Surgical Instruments Nationwide View Details β†’

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Apr 13, 2017 Other Medical Devices Nationwide View Details β†’

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Feb 1, 2013 Infusion Pumps Nationwide View Details β†’

The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.

Jun 2, 2017 Implants & Prosthetics Nationwide View Details β†’

The connection between the Female Luer and the NanoClaveΒΏ manifold has the potential for developing a leak.

May 30, 2017 Surgical Instruments View Details β†’

The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.

Jun 2, 2017 Implants & Prosthetics Nationwide View Details β†’

If the gantry module is replaced after original installation the configuration settings may be missing. The identified risk for this issue is electrical safety for technicians doing maintenance on the X-ray generator.

May 23, 2017 Diagnostic Equipment View Details β†’

The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.

Jun 2, 2017 Implants & Prosthetics Nationwide View Details β†’

The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.

Jun 2, 2017 Implants & Prosthetics Nationwide View Details β†’