Drive P703Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00822383979434), received between Jan 4, 2023 and Dec 29, 2025 — classified as 3 injuries, 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryDec 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY THE END USER'S DAUGHTER WHO STATED THAT THE END USER FELL BETWEEN THE BED RAILS AND BUMPERS ONTO THE FLOOR. IT WAS UNCLEAR HOW THE BED AND ACCESSORIES WERE ASSEMBLED. THE END USER HAD BRUISING TO THEIR SHOULDER AND A CUT ACROSS THEIR TEAR DUCT ON THE LEFT EYE. SHE WENT TO THE EMERGENCY ROOM AND HAD X-RAYS AND A CT SCAN, AND WAS PRESCRIBED AN ANTIBIOTIC CREAM FOR THE CUT ACROSS THE TEAR DUCT. 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 23919163 ↗
• InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY THE END USER'S DAUGHTER WHO STATED THAT THE END USER FELL BETWEEN THE BED RAILS AND BUMPERS ONTO THE FLOOR. IT WAS UNCLEAR HOW THE BED AND ACCESSORIES WERE ASSEMBLED. THE END USER HAD BRUISING TO THEIR SHOULDER AND A CUT ACROSS THEIR TEAR DUCT ON THE LEFT EYE. SHE WENT TO THE EMERGENCY ROOM AND HAD X-RAYS AND A CT SCAN, AND WAS PRESCRIBED AN ANTIBIOTIC CREAM FOR THE CUT ACROSS THE TEAR DUCT. 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 23831704 ↗
• InjuryMar 17, 2023Component Missing; Device Dislodged or Dislocated; Component Missing; Device Dislodged or Dislocated

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED BY AN ASSISTED LIVING FACILITY, WHICH REPORTED THAT "AN END USER WENT TO SWING HER LEGS OUT OF BED AND CAUGHT HER LEGS ON THE BED FRAME, REQUIRING STITCHES AND HIGH LEVEL OF CARE." IT WAS REPORTED THAT THE BED WAS MISSING THE END CAPS ON THE FRAME SEGMENTS, REVEALING THE METAL EDGE. THE END CAPS ARE INTENDED TO PROTECT THE END USER FROM CONTACT WITH THE METAL EDGE. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Laceration(s)

  MAUDE report 16566220 ↗
• MalfunctionJan 4, 2023Fire; Sparking; Fire; Sparking

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BARIATRIC BED BY A DISTRIBUTOR, WHO STATED THAT "DURING OPERATION OF THE BED THE POWER CORD WAS PINCHED AND CAUSED A SPARK, WHICH CAUSED A FIRE." GIVEN THAT THE FIRE WAS CAUSED BY A PINCHED POWER CORD, DRIVE HAS CONFIRMED THAT THERE WAS NO REPORTED DEFECT OR ISSUE WITH THE DESIGN OR MANUFACTURE OF THE UNIT. THERE WAS NO REPORT OR EVIDENCE OF ILLNESS, INJURY OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16096836 ↗