Arthrex® AR-1560Recalls & reported problems
Arthrex, Inc. · PIVOTPOST & CLAMP · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867095182), received between Jun 19, 2024 and Jan 15, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Material Twisted/Bent1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 15, 2025Break; Break
ON 12/19/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS-06739377 THAT AN AR-1560 PIVOT POST AND CLAMP HAD THE PIECE THAT MAKES IT SWIVEL BREAK OFF. NO FURTHER INFORMATION WAS PROVIDED. THIS WAS DISCOVERED DURING A PROCEDURE. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Insufficient Information
MAUDE report 21157616 ↗MalfunctionJun 19, 2024Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE POST IS NOT SECURE; IT IS BENDING AT THE ROTATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19568082 ↗
Other TABLE AND ATTACHMENTS, OPERATING-ROOM devices
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- Arthrex® AR-1644Arthrex, Inc. · Table and attachments, operating-room5 reports
- Leg holder 100380A0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1560-02Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1500Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Pair of leg plates 113373BCMAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Kneeling frame 100704D0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
- Traction boot, adult 10018800MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.