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VIVE LVA1028LRecalls & reported problems

Vive Health LLC · Suction Grab Bar 16 Inch Large · 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 00818323026221), received between Aug 29, 2019 and Aug 29, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1
  • Physical Resistance/Sticking1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryAug 29, 2019Detachment of Device or Device Component; Physical Resistance/Sticking

    A CUSTOMER LEFT A COMMENT STATING, "WORSE PRODUCT I EVER BOUGHT IT STUCK AFTER SHOWERING I GRAB THE HANDLE AND IT CAME OFF, I HURT MYSELF." FDA SAFETY REPORT ID# (B)(4).

    Patient problems: Pain

    MAUDE report 8949647 ↗

Other Aid, Transfer devices

All Aid, Transfer devices →

Sources and updates

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