AXSOS 627542Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327174915), received between Jul 18, 2018 and Jul 18, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 18, 2018Break

  AS REPORTED ON MAUDE REPORT MW5077828 VIA THE FDA: "MY MOTHER (B)(6) IS A (B)(6) LADY. PRIOR TO HER INJURY, SHE HAS ALWAYS BEEN A VERY ACTIVE WOMAN, SEWING, GARDENING, CANNING AND FREEZING HER PRODUCE. SHE ATTENDED MEETINGS TWICE AS A VOLUNTEER WITH THE (B)(6) CLUB AND HELPED AT THEIR FUNDRAISING BENEFITS. SHE LOVED TO GO TO THE CASINO AND GO SHOPPING. IN (B)(6) 2017, SHE SUSTAINED A RIGHT HIP INJURY FROM A FALL. SURGERY WAS DONE AND SHE RECOVERED NICELY; RESUMING ALL FORMER ACTIVITIES. ON (B)(6) 2017, THE DAY BEFORE HER (B)(6) BIRTHDAY, SHE FELL IN THE KITCHEN AND BROKE HER RIGHT FEMUR BELOW THE PREVIOUS INJURY; SUSTAINING A SPIRAL FRACTURE WHICH REQUIRED SURGICAL PLACEMENT OF A STRYKER FEMORAL TITANIUM PLATE TO STABILIZE THE BONE AND ALLOW HER LEG TO HEAL. SHE CONVALESCED AT HOME WITH DAILY THERAPY AND NURSE'S VISITS SUPPLIED BY (B)(4). (B)(6) SAW HER SURGEON, (B)(6) MD, ON (B)(6) 2018 AT WHICH TIME HE PRONOUNCED HER FEMUR HEALED AND TOLD HER SHE COULD RESUME ALL ACTIVITIES WITH NO RESTRICTIONS. ON (B)(6) 2018, SHE SAW HER GP FOR A YEARLY PHYSICAL AND WAS TOLD SHE WAS FIT AS A FIDDLE. SHE HAD ONE FINAL APPOINTMENT WITH DR. (B)(6) ON (B)(6) 2018; TELLING HER SHE DIDN'T HAVE TO "VI

  Patient problems: Failure of Implant

  MAUDE report 7700777 ↗