Drive 13003Recalls & reported problems
Drive Devilbiss Healthcare · Overbed Table,Dlx.Non-Tilt,1/cs · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383102979), received between Oct 22, 2022 and Oct 22, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 22, 2022Unintended Movement; Unintended Movement
WE RECEIVED THE EMAIL MEDWATCH REPORT # 2438477-2022-00032 FROM OUR CUSTOMER DRIVE DEVILBISS HEALTHCARE ON (B)(6) 2022, DRIVE EMAIL CONTENT AS BELOW: THE MEDICAL DEVICE INVOLVED IN THE INCIDENT IS A OVERBED TABLE, MODEL NUMBER # 13003. THE SERIAL NUMBER IS (B)(4). PLEASE REFER TO THE MEDWATCH REPORT FOR INFORMATION ABOUT THE EVENT. AS OF TODAY, THE PRODUCT IN QUESTION HAS NOT BEEN RETURNED TO DRIVE MEDICAL FOR EVALUATION. DRIVE ATTACHMENT CONTENT AS BELOW: ON (B)(6) 2022, DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING AN OVERBED TABLE. THE END USER REPORTED AS FOLLOWS: "TABLE SPRING SPRUNG CAUSING TABLE TO FLY UP WITH GREAT FORCE. STUCK HIGH NOW. VERY DANGEROUS." THE END USER DID NOT SUSTAIN ANY INJURY. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT. AS THE MANUFACTURER, JUMAO REPLIED AS BELOW: DRIVE MEDWATCH REPORT #2438477-2022-00032, INCIDENT DEVICE: OVERBED TABLE, MODEL NUMBER # 13003, SERIAL NUMBER # (B)(4), THE INVESTIGATION OF INCIDENT IS DESCRIBED AS BELOW: HOW MANY SIMILAR MDR, COMPLAINTS, OR SERVICE REQUESTS FOR THE SAME PRODUCT HAVE YOU RECEIVED OVER THE PAST THREE (3) YEARS? WE HAVE NOT RECEIV
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15656105 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.