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Drive RTL13084Recalls & reported problems

Drive Devilbiss Healthcare · Grab Bar SuctionCup,ADJ,19 3/4",1EA,3/CS · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383246529), received between Mar 14, 2019 and Mar 14, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • Fall1
  • Injury1

Recent adverse event reports

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

  • InjuryMar 14, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

    (B)(4) IS TH INITIAL IMPORTER OF THE DEVICE WHICH IS A GRABBER. THE END-USER GRABBED THE BAR WHEN THE GREEN INDICATOR WAS ACTIVATED. HOWEVER THE PIN WASN'T IN THERE AND THE PERSON FELL HE WENT TOT HE EMERGENCY ROOM. THE PATIENT WAS INJURED. C3- C6 BONES AND IS CURRENTLY DOING PHYSICAL THERAPY. HE MAY NEED SURGERY LATER ON. THE PATIENT IS 6FT AND (B)(6). HE HAS BEEN USING THE DEVICE FOR 2 MONTHS.

    Patient problems: Fall; Injury

    MAUDE report 8422031 ↗

Other ADAPTOR, HYGIENE devices

All ADAPTOR, HYGIENE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.