Isolibrium 2972 (REF 297205550001)Recalls & reported problems
Stryker Corporation · Class 2
- 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 07613327390049), received between Jan 23, 2024 and Jan 23, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
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.
MalfunctionJan 23, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE AC CURRENT. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18565189 ↗
Other BED, PATIENT ROTATION, POWERED devices
- Isolibrium 2972Stryker Corporation · BED, PATIENT ROTATION, POWERED1 recall17 reports
- Isolibrium 297300000000Stryker Corporation · BED, PATIENT ROTATION, POWERED25 reports
- Isolibrium 2971Stryker Corporation · BED, PATIENT ROTATION, POWERED11 reports
- Pronova-O2 1Turn Medical, LLC · Bed, Patient Rotation, Powered2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.