Drive P503Recalls & reported problems
Drive Devilbiss Healthcare · Prime Care Model P503 · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383982823), received between Jul 17, 2024 and Jul 26, 2024 — classified as 2 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available2
Patient problems
- Laceration(s)2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 26, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY THE PROVIDER WHO STATED THE BED WAS MISSING A COVER ON THE ENDCAP OF THE METAL BED FRAME. THE END USER RECEIVED A CUT TO THEIR SHIN THAT REQUIRED STITCHES WHEN THEY FELL UNDER THE BED AND CAUGHT THEIR LEG ON THE EDGE. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Laceration(s)
MAUDE report 19835077 ↗InjuryJul 17, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY THE PROVIDER WHO STATED THE BED WAS MISSING A COVER ON THE ENDCAP OF THE METAL BED FRAME. THE END USER RECEIVED A CUT TO THEIR SHIN THAT REQUIRED STITCHES WHEN THEY FELL UNDER THE BED AND CAUGHT THEIR LEG ON THE EDGE. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Laceration(s)
MAUDE report 19763898 ↗
Other Bariatric bed devices
- Medline MDR107004Medline Industries, Inc. · Bariatric bed110 reports
- MV3 5900Stryker Corporation · Bariatric bed1 recall41 reports
- Medline FCEALTMAXXMedline Industries, Inc. · Bariatric bed84 reports
- Drive 15300BV-PKGDrive Devilbiss Healthcare · Bariatric bed2 reports
- Synergy® Surface P6881CAPHill-Rom, Inc. · Bariatric bed2 reports
- Joerns Bari10AJoerns Healthcare, LLC · Bariatric Bed2 reports
- Drive 15300Drive Devilbiss Healthcare · Bariatric bed1 report
- INVACARE® BAR600 BARIATRIC BED BAR600IVCInvacare Corporation · Bariatric Bed1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page