Arthrex® AR-1560-02Recalls & reported problems
Arthrex, Inc. · PIVOTPOST REPLACEMENT · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888867095205), received between Oct 11, 2023 and May 30, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
- Positioning Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 30, 2025Positioning Failure; Positioning Failure
ON 05/12/2025, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-1560-02 PIVOT POST DOESNT LOCK TIGHTLY. THIS OCCURRED DURING USE IN A CASE WITH NO PATIENT EFFECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22114376 ↗MalfunctionJun 18, 2024Break; Break
IT WAS REPORTED THAT THE BLACK LEVER ON TOP OF THE AR-1560-02 HAS BROKEN OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19564180 ↗MalfunctionJun 10, 2024Break; Break
ON 05/09/2023 IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-1560-02 PIVOT POST ROTATOR IS BROKEN. THIS WAS DISCOVERED DURING AN UNSPECIFIED TIME WITH NO PATIENT EFFECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19503288 ↗MalfunctionOct 11, 2023Break; Break
ON 9/13/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS-06030096 THAT AN AR-1560-02 PIVOTPOST REPLACEMENT SNAPPED OFF DURING A CASE. THE CLIP BROKE OFF TO WHERE IT IS UNUSABLE, AS IT WILL NOT PIVOT AT ALL. THIS WAS DISCOVERED DURING AN UNSPECIFIED PROCEDURE, WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17914730 ↗
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- Arthrex® AR-1644Arthrex, Inc. · Table and attachments, operating-room5 reports
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- Arthrex® AR-1500Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Pair of leg plates 113373BCMAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Traction boot, adult 10018800MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
- Leg holder 100165A0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
- Arthrex® AR-1560Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM2 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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