Radiolucent ChairRecalls & reported problems
Eos Imaging · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 03663999000061), received between Sep 18, 2017 and Sep 18, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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
- Device Operates Differently Than Expected1
- Device-Device Incompatibility1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 18, 2017Device Operates Differently Than Expected; Device-Device Incompatibility; Device Operates Differently Than Expected; Device-Device Incompatibility
ON (B)(6) 2017, (B)(4), EOS IMAGING REGIONAL APPLICATION SPECIALIST, RECEIVED A CALL FROM (B)(6), DIRECTOR OF RADIOLOGY AT (B)(6). IT WAS INITIALLY REPORTED THAT WHILE MOVING A PATIENT SEATED IN AN EOS RADIOLUCENT CHAIR INTO THE EOS SYSTEM GANTRY THE CHAIR FLIPPED OVER BACKWARDS. FORTUNATELY, THEY HAD 2 STAFF MEMBERS IN THE ROOM AND THE PATIENT WAS NOT INJURED. ADDITIONAL INFORMATION WAS REQUESTED BY (B)(4) AND RECEIVED THE SAME DAY FROM (B)(6), IT WAS REPORTED THE FOLLOWING: THE PATIENT WAS STRAPPED INTO THE CHAIR WHEN THIS HAPPENED. THEY WERE ATTEMPTING TO PUSH THE PATIENT UP THE RAMP AND INTO THE GANTRY. THE REAR WHEELS GOT CAUGHT ON THE ENTRY RAMP WHICH CAUSED THE CHAIR TO TIP OVER. PATIENT'S FAMILY WAS IN THE EOS ROOM AT THE TIME. THE ONSITE PHYSICIAN AND NURSES EXAMINED THE PATIENT AND NO PHYSICAL INJURIES WERE NOTICED. THERE WERE 3 TECHNOLOGISTS ATTEMPTING TO MOVE THE PATIENT INTO THE GANTRY WITH ONE AT EITHER SIDE AND THE OTHER AT THE FRONT OF THE CHAIR. THE CHAIR FELL COMPLETELY OVER AND INTO THE GANTRY. THEY MANAGED TO GET THE CHAIR UPRIGHT AND THE PATIENT WAS REMOVED FROM THE ROOM. PATIENT DETAILS ARE AS FOLLOWS: AGE-(B)(6). GENDER- MALE. WEIGHT- (B)(6). HEIGHT-154.9 CM.
Patient problems: Fall
MAUDE report 6872886 ↗
Other Chair, With Casters devices
- MEDLINE MDS808210AREMedline Industries, Inc. · CHAIR, WITH CASTERS115 reports
- MEDLINE MDS808210ABEMedline Industries, Inc. · CHAIR, WITH CASTERS75 reports
- Zippie Voyage Voyage; Voyage VIPSunrise Medical (US) LLC · Chair, With Casters1 recall9 reports
- Ki TykeKi Mobility, LLC · Chair, With Casters1 recall0 reports
- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- MEDLINE MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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