Skip to content

Drive RTL13083Recalls & reported problems

Drive Devilbiss Healthcare · Grab Bar,Suction,WHT/BEIG,12",1EA,3/CS · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00822383580876), received between Feb 15, 2019 and Feb 15, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • Damage to Ligament(s)1
  • Fall1

Recent adverse event reports

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

  • InjuryFeb 15, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

    (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A GRAB BAR. THE END-USER ACQUIRED THE DEVICE FOR ASSISTANCE IN AND OUT OF BATHTUB. SHE WAS USING THE DEVICE PRIOR TO UNDERGOING A TOTAL KNEE REPLACEMENT SURGERY ON (B)(6) 2018. THE PRODUCT DETACHED FROM WALL WHILE END USER WAS GETTING OUT OF THE SHOWER. THE PATIENT WAS DIAGNOSED WITH TORN PATELLAR TENDON WHICH REQUIRED SURGERY AND A KNEE BRACE FOR 8 WEEKS. THIS PROCEDURE TOOK PLACE ON (B)(6) 2019.

    Patient problems: Damage to Ligament(s); Fall

    MAUDE report 8344034 ↗

Other AID, TRANSFER devices

All AID, TRANSFER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page