inforMED
InjuryKWD

HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY

Received May 4, 2020

Report 3004154314-2020-00002 · MDR key 10022814

Device

Generic name

Toe Hemicap

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • No Code Available
  • No Code Available

Narrative

Additional Manufacturer Narrative

THE PATIENT INQUIRED IF OTHER PATIENTS UNDERGO A PHYSICAL THERAPY FOLLOWING THE HEMICAP SURGERY AND SHE IS ALSO CONCERNED ABOUT NOT BEING ABLE TO WEAR HEELS EVEN AFTER 5 MONTHS OUT. THE REASON FOR PATIENT'S COMPLAINT CANNOT BE ASCERTAINED DUE TO LACK OF INFORMATION REQUIRED FOR THE INVESTIGATION. SINCE NO DEVICE OR LOT INFORMATION WAS PROVIDED, A REVIEW OF DEVICE MANUFACTURING RECORDS COULD NOT BE CONDUCTED. SEVERAL FACTORS SUCH AS STRESS/ PHYSICAL LOADS ON THE IMPLANTS, VASCULARITY OF THE IMPLANTATION SITE, SURGICAL TECHNIQUES EMPLOYED DURING IMPLANTATION, PATIENT FACTORS (SUCH AS AGE, PRE-EXISTING CONDITIONS, CURRENT STATE OF THE IMMUNE SYSTEM, BONE QUALITY, AND SENSITIVITY TO DEVICE MATERIALS), AND PATIENT POST-OP COMPLIANCE TO REHABILITATION PROCEDURES ETC. CAN HAVE IMPACT ON THE FUNCTIONAL EFFECTIVENESS OF THE IMPLANTED DEVICES. THE PATIENT WAS PROVIDED A POST-OP PROTOCOL AND WAS ADVISED TO CONSULT THEIR TREATING SURGEON FOR FURTHER CONCERNS REGARDING IMPLANT AND PHYSICAL THERAPY. THE COMPLAINT WILL BE CLOSED AT THIS TIME AND ANY NEW INFORMATION RECEIVED WILL BE REVIEWED AND REPORTED ACCORDINGLY.

Description of Event or Problem

THE PATIENT REACHED OUT TO ARTHROSURFACE VIA WEBSITE TO INQUIRE REGARDING PHYSICAL THERAPY AFTER RECEIVING THE HEMICAP. SHE RECEIVED THE IMPLANT FIVE MONTHS AGO AND CURRENTLY CANNOT WEAR HEELS.