HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY
Received May 4, 2020
Report 3004154314-2020-00002 · MDR key 10022814
Device
Generic name
Toe Hemicap
Manufacturer
Arthrosurface, Inc.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.