12019Feb
TrackMy Solutions is now an ADP Integrator with Allscripts EHR products

TrackMy Solutions is now an ADP Integrator with Allscripts EHR products

Allscripts® is a leader in EHR integration and healthcare information technology solutions that advance clinical, financial and operational results across an open platform. TrackMy® Solutions is an ADP Integrator with Allscripts Professional EHR and Allscripts TouchWorks EHR products for TrackMy® Implants. Through this program, we continue our progress for a leading edge Smart on FHIR…

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222019Jan
News & Views Links

News & Views Links

Medex Cardio-Pulmonary, doing business as Smiths Medical, Recalls Sterile Saline and Sterile Water 2/5/19 | Smiths Medical is recalling the sterile saline and sterile water products for inhalation due to the potential exposure to infectious agents (bacillus infantis and staphylococcus epidermidis) because of damage to the containers used to package the finished products. READ MORE…….

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212019Jan
Healthcare advancement for 2019!

Healthcare advancement for 2019!

2019 represents the potential for another great year in improving healthcare!  At TrackMy Solutions, we are already hard at work to improve our products and continue to challenge the status quo of technology and interoperability. With the continued push of consumer-driven healthcare and empowering patients/consumers to manage their health – we have kicked off a…

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112019Jan
Stryker Class 2 Recall

Stryker Class 2 Recall

Stryker issued a Class 2 Device Recall of its Tritanium Posterior Lumbar cage in November/December of 2018. This device originally received clearance from the FDA in November of 2015. Stryker’s reason for the recall is listed as: “The surgical technique is being updated to caution against misue due to reports of cage fractures occurring intraoperatively…

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72019Jan
Happy New Year – Here’s a list of Medical Device Recalls from 2018.

Happy New Year – Here’s a list of Medical Device Recalls from 2018.

GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit 12/12/18 Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect 11/27/18 Zimmer Biomet, Inc. Recalls Spinal Fusion and Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness 11/26/18 Oscor Recalls…

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302018Nov
The Bleeding Edge Documentary Screening

The Bleeding Edge Documentary Screening

On December 1st we will be hosting a private screening for The Bleeding Edge, a documentary on Netflix about the dangers of medical device implants. We look forward to spreading the word of ASHES Non-Profit president Angie Firmalino, who was featured in the movie. Read about her personal story, along with how she and the…

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72018Oct
Welcoming Dr. Aakash Shah to TrackMy Solutions!

Welcoming Dr. Aakash Shah to TrackMy Solutions!

We are very excited to welcome a new partner to the TrackMy Solutions team, Dr. Aakash Shah. Dr. Shah is an Orthopaedic Surgeon at Menorah Medical Center in Overland Park, Kansas. He is a Board Certified Orthopaedic surgeon as well as Board Certified in Sports Medicine. All of us here at TrackMy Solutions are poised…

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62018Jun
Medical Device UDI & Patients

Medical Device UDI & Patients

Every year more and more people are getting medical device implants installed in their body. This includes hips, knees, cardiac devices, cataract lenses and more. These devices are amazing life saving technological advancements. While these are on the rise, sadly recalls are too. When a patient has a device installed they leave the surgery center,…

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302018Apr
Healthcare Technology & Medical Device Implants

Healthcare Technology & Medical Device Implants

The amount of technology we have available to us in the world today is astounding. Wherever we go it’s around us, with us, and in many cases, watching us. This is especially true in healthcare. Technology has not only made things safer and more efficient, but has changed the way providers deliver care to their…

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302018Mar
Office of Women’s Health

Office of Women’s Health

OWH-Funded Research: Medical Device Safety The FDA Office of Women’s Health awards research grants for 1-2 year studies to support FDA regulatory decision-making and advance the science of women’s health. OWH has funded research projects that address health issues affecting women across their lifespan. Read the full article here.

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132018Mar
FDA recently approved devices

FDA recently approved devices

FDA has recently approved the following devices to be marketed: PulseRider Aneurysm Neck Reconstruction Device (“PulseRider”) – H160002 The PulseRider is a permanent nitinol (nickel titanium) self-expanding stent implant for the treatment of wide-necked aneurysms located at or near branching areas of arteries in the brain. The device’s Y or T shape provides support for…

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