Kneeling frame 100704D0Recalls & reported problems
MAQUET GmbH · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04046768039278), received between Aug 22, 2025 and Aug 22, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Premature Separation” (2 reports).
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
- Premature Separation2
Patient problems
- Bone Fracture(s)2
- Bruise/Contusion2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 22, 2025Premature Separation; Premature Separation
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR ACCESSORIES ¿ 100704D0 - DEVICE FOR SPINAL SURGERY. AS STATED, DURING THE PATIENT¿S TRANSFER FROM THE OPERATING TABLE TO THE BED, THE OR TABLE WAS INTENTIONALLY MOVED BY A NURSE. AS A RESULT, THE FRAME DETACHED FROM ITS HINGE POINTS AND FELL APPROXIMATELY 80 CM ONTO THE NURSE¿S LEFT FOOT AND AGAINST THE LEFT HAND, RESULTING IN A FRACTURE OF THE THIRD TOE AND A SLIGHT BRUISE TO THE HAND. WE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY OF THE USER. REF # (B)(4).
Patient problems: Bone Fracture(s); Bruise/Contusion
MAUDE report 22871848 ↗InjuryAug 22, 2025Premature Separation; Premature Separation
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR ACCESSORIES ¿ 100704D0 - DEVICE FOR SPINAL SURGERY USED WITH 118010A0 - BASIS TABLE TOP, INDIVIDUAL CONFIGURATION. AS STATED, DURING THE PATIENT¿S TRANSFER FROM THE OPERATING TABLE TO THE BED, THE OR TABLE WAS INTENTIONALLY MOVED BY A NURSE. AS A RESULT, THE FRAME DETACHED FROM ITS HINGE POINTS AND FELL APPROXIMATELY 80 CM ONTO THE NURSE¿S LEFT FOOT AND AGAINST THE LEFT HAND, RESULTING IN A FRACTURE OF THE THIRD TOE AND A SLIGHT BRUISE TO THE HAND. WE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY OF THE USER.
Patient problems: Bone Fracture(s); Bruise/Contusion
MAUDE report 22870328 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.