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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

The MYLAΒΏ server could slow down due to the volume (weight) of the data to manage and it could also stop processing, impacting the server start-up phase. The problem occurs in high volume settings. The MYLA server slows down and will stop processing completely if any task requires more than 5 minutes to complete. The server then fails to reboot and requires service, provided remotely or on-site

Apr 14, 2015 Surgical Instruments View Details β†’

Integra LifeSciences Corporation is recalling Integra's Camino ICP Monitor (CAM 02) & Licox PtO2 Monitor ( LCX02 & LCX02R) due to complaints that the audible speaker malfunctions.

Apr 14, 2015 Diagnostic Equipment View Details β†’

Stryker received four customer complaints reporting that inside the box labeled part #6476-8-260 (Kinemax Stem Extenders, 80 mm) there was a different part #6476-8-250 (Kinemax Stem Extenders, 40 mm.

Feb 27, 2015 Implants & Prosthetics Nationwide View Details β†’

The firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned.

Mar 11, 2015 Other Medical Devices Nationwide View Details β†’

Devices were placed in a shipper carton without the appropriate number of the Instructions for Use (IFU). Packaging specifications require that each sales unit is accompanied by an IFU. Only one IFU was present in the shipper carton, instead of one IFU per each of the two sales units.

Apr 21, 2015 Surgical Instruments View Details β†’

Under certain circumstances the patient Demographics in a report exported into the EMR may not match the demographics shown in the corresponding Synapse CV clinical report.

Feb 4, 2015 Diagnostic Equipment Nationwide View Details β†’

Some rods may not meet the appropriate traceability requirements including the lot number. Some rods were found to not include the product identification number (product number and lot number) marked directly on the rod. The lack of marking interrupts the ability to maintain traceability of the device.

Apr 9, 2015 Other Medical Devices Nationwide View Details β†’

The heart rate could be calculated from pacer pulses without indication that pacemaker detection is OFF in some combinations of Bx50 monitors, a PDM, and CIC/CSCS. Then the monitor does not show the Pacer Off message and there may not be an alarm for asystole. Undetected asystole could result in irreversible changes in the patientΒΏs condition and delayed or missed life sustaining patient treatment

May 4, 2015 Diagnostic Equipment View Details β†’

Certain Dimension Integrated Chemistry Systems Instrument Power Configurations may have been installed with a non-standard instrument power plug.The use of a non-standard plug configuration as described may lead to a potential electrical hazard. The likelihood of potential clinical impact or injury due to this issue is extremely low.

Apr 2, 2015 Diagnostic Equipment View Details β†’

Beckman Coulter has received an increased number of complaints related to Hemoglobin (HGB) on UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems. The use of the DxH Diluent lots listed in the recall notice may eventually result in a compromised HGB chamber.

Apr 13, 2015 Other Medical Devices View Details β†’

The input power can fail even though the power source at the wall has not been interrupted. In addition, there is the potential for the qube Compact Monitor to fail to turn on. This is a retrospective recall related to a recall initiated in 2012 (Z-0403-2013).

May 8, 2015 Diagnostic Equipment View Details β†’