Axiom Back AXDLRecalls & reported problems
Ki Mobility, LLC · AXIOM DEEP LATERAL BACKREST · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850013379170), received between Apr 18, 2024 and Apr 18, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Intracranial Hemorrhage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 18, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
DURING TRANSFER OF THE PATIENT FROM THE CHAIR, THE TRANSFER FAILED AND THE PATIENT FELL BACKWARDS INTO THE CHAIR. THIS RESULTED IN THE PATIENT STRIKING THE BACKREST AND THE BACKREST DISCONNECTED ALLOWING THE PATIENT TO FALL BACKWARDS AND HIT THEIR HEAD. THEY SAID THEY BELIEVE THE BACKREST DISCONNECTED BECAUSE IT WAS UNLATCHED, BUT THEY DON'T KNOW BY WHOM AND WHEN.
Patient problems: Intracranial Hemorrhage
MAUDE report 19133218 ↗
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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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