CARDINAL HEALTH CA901YTHRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50885380050372), received between Dec 8, 2016 and Dec 8, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Split” (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.

• InjuryDec 8, 2016Split

  BASED ON THE CUSTOMER¿S HUSBANDS STATEMENT, THE METAL WHERE THE HEIGHT IS ADJUSTED ON THE CRUTCH SPLIT CAUSING HIS WIFE TO FALL.  HE STATED SHE ONLY USES THEM WHEN SHE TRANSITIONS FROM A KNEE WALKER TO A RECLINER AND SHE ONLY TAKES TWO "BABY STEPS." WHEN THE CRUTCH SPLIT SHE FELL FORWARD AND HIT HER HEAD ON A DRESSER THAT IS IN THE ROOM AND SPLIT HER HEAD OPEN.  EMT¿S WERE CALLED AND SHE WAS TRANSPORTED TO (B)(6) HOSPITAL. SHE SUFFERED A MILD NECK SPRAIN, BANGED HER BAD FOOT ON THE FLOOR AND RECEIVED SIX STITCHES FOR THE WOUND ON HER HEAD.

  Patient problems: Fall

  MAUDE report 6154560 ↗