Probasics RLATBLRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815067071814), received between Apr 10, 2020 and Apr 10, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Structural Problem” (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. How this data works · Data updated Oct 13, 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.

• InjuryApr 10, 2020Structural Problem; Structural Problem

  THE END-USER ALLEGES THAT THE PRODUCT COLLAPSED ON HER SECOND DAY OF USE AND SHE FELL FRACTURING HER FEMUR REQUIRING OPEN REDUCTION WITH INTERNAL FIXATION. PER END-USER COUNSEL: PLAINTIFF IS SLIM (WELL UNDER 250). THE ROLLATOR DID NOT BREAK, THERE ARE NO BROKEN PIECES, THERE WAS NO MANUFACTURING DEFECT. PLAINTIFF WAS WALKING WITH IT INSIDE AT HER HOME AND IT CLOSED UP ON HER. HE THINKS THAT PLAINTIFF PICKED IT UP FROM THE STORE AND BELIEVES THAT IT WAS GIVEN TO PLAINTIFF FULLY ASSEMBLED. CLAIMING DESIGN DEFECT AS IT DOES NOT HAVE A LOCKING MECHANISM TO PREVENT THIS TYPE OF INCIDENT. ON 02/21/2020 CHB WAS INFORMED OF INCIDENT. ON 03/30/2020 CHB WAS INFORMED OF INJURY.

  Patient problems: Bone Fracture(s)

  MAUDE report 9947699 ↗