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DRIVEMEDICAL SSP216DDA-ELRRecalls & reported problems

Drive Devilbiss Healthcare · Pressure PreventionLTC and Hospice Product Description: Spec.Furn.,Grav8 Mattress 76"w/RR,1/EA · Class 1

All models of DRIVEMEDICAL (111)

Data updated Oct 18, 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 00822383140421), received between Apr 22, 2021 and Apr 22, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

Device problems

  • Break1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryApr 22, 2021Break; Break

    DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A TRANSPORT CHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE AWAITING ADDITIONAL DATASETS AS WELL. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL FILE A FOLLOW-UP WHEN ADDITIONAL INFORMATION IS AVAILABLE. THE SPECIFIC NATURE OF THE PRODUCT ISSUE IS UNKNOWN. THE USER REPORTEDLY ACQUIRED AN INJURY TO THE SPINE THAT NEEDED TREATMENT. THE SPECIFIC TYPE OF TREATMENT IS UNKNOWN AT THIS TIME.

    Patient problems: Insufficient Information

    MAUDE report 11705920 ↗

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Sources and updates

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