Arthrex® AR-1627-10Recalls & reported problems
Arthrex, Inc. · INTUBATION PAD & PLATE · Class 1
Data updated Oct 16, 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 00888867020269), received between Aug 29, 2023 and Aug 29, 2023 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
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.
MalfunctionAug 29, 2023
SURGICAL CASE: RIGHT SHOULDER OPEN REDUCTION. DURING SURGICAL CASE, PATIENT IN BEACH CHAIR POSITION, BEACH CHAIR MALFUNCTIONED: CHANGING THE PATIENT¿S POSITION FROM SITTING UPRIGHT TO LAYING WITHOUT INTENTION OF THE SURGICAL TEAM. SURGERY WAS COMPLETED AS PLANNED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17640996 ↗
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- ALLEN 108001Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall3 reports
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- MAYFIELD® A1018Integra Lifesciences Corporation · Operating Room Accessories Table Tray36 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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