Skip to content

Arthrex® AR-2924BCHRecalls & reported problems

Arthrex, Inc. · BioComposite 2.4mm Mini Hip PushLock · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00888867311305), received between May 10, 2021 and Feb 7, 2024 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Break” (4 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 1 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break4
  • Crack1
  • Device Dislodged or Dislocated1
  • Explosion1

Patient problems

  • Insufficient Information4
  • Foreign Body In Patient1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 7, 2024Break; Break

    ON (B)(6) 2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AN AR-2924BCH BIOCOMPOSITE 2.4MM MINI HIP PUSHLOCK BROKE. THIS WAS DISCOVERED DURING A HIP LABRAL REPAIR PROCEDURE ON (B)(6) 2024. ALL THE BROKEN FRAGMENTS WERE REMOVED. NO FURTHER INFORMATION WAS PROVIDED. ADDITIONAL INFORMATION REQUESTED.

    Patient problems: Insufficient Information

    MAUDE report 18660259 ↗
  • MalfunctionJan 2, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ON 12/4/2023, IT WAS REPORTED BY A DISTRIBUTOR VIA (B)(4) THAT AN AR-2924BCH BIOCOMPOSITE 2.4MM MINI HIP PUSHLOCK PULLED OUT. THIS WAS DISCOVERED DURING A HIP LABRUM PROCEDURE ON (B)(6) 2023. TWO OTHER MINI HIP PUSHLOCK WORKED FINE BUT THE THIRD PULLED OUT.

    Patient problems: Insufficient Information

    MAUDE report 18424776 ↗
  • MalfunctionDec 13, 2021Break

    ON (B)(6) 2021, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT TWO AR-2924BCH IMPLANTS BROKE ON INSERTION DURING A HIP SCOPE WITH A LABRAL REPAIR. THE FIRST IMPLANT BROKE ON INSERTION. ALL WAS RETRIEVED. A SECOND IMPLANT WAS USED IN THE SAME LOCATION AND IMPLANTED FINE. A THIRD IMPLANT WAS USED DURING THIS PROCEDURE BUT ALSO BROKE DURING INSERTION. THE TOP PART BROKE OFF AND IT WAS RETRIEVED. THE REMAINDER OF THE ANCHOR STAYED SEATED AND THE SURGEON DETERMINED IT HAD SUFFICIENT FIXATION THEREFORE HE ELECTED TO LEAVE IT IN THE PATIENT. THE PROCEDURE WAS COMPLETED WITH NO FURTHER ISSUES. THE PATIENT IS FINE TO DATE.

    Patient problems: Foreign Body In Patient

    MAUDE report 12983462 ↗
  • MalfunctionAug 3, 2021Break; Crack

    IT WAS REPORTED THAT DURING A HIP ARTHROSCOPIC PROCEDURE WITH LABRAL REPAIR, THE SURGEON USED THE 2.4MM X 8.9MM BIOCOMPOSITE HIP PUSHLOCKS, AR-2924BCH AND THE FIRST PUSHLOCK WAS IMPLANTED WITH NO ISSUES. THE SURGEON THEN USED THE AR-2924DHS-1 DISPOSABLE KIT TO PREPARE THE BONE SOCKET AND THERE WERE QTY. 4 OF THE 2.4 HIP PUSHLOCKS THAT CRACKED ON THE FIRST IMPACT. THE SURGEON PREPARED THE BONE SOCKET EXACTLY THE SAME WAY AND ALSO TOOK EXTRA PRECAUTION TO MAKE SURE THE ANCHOR WAS IN LINE WITH THE SOCKET BEFORE MALLETING IN THE PUSHLOCK AND CYCLED THE DRILL EACH TIME TO MAKE SURE THERE WAS NOT BONE DEBRIS IN THE SOCKETS. THE MATERIAL FROM EACH ANCHOR THAT BROKE OFF WAS FOUND AND REMOVED FROM THE PATIENT. THE PATIENT WAS NOT AFFECTED BY THE ANCHORS BREAKING. THE CASE WAS COMPLETED BY USING TWO 2.9MM HIP PUSHLOCKS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12267234 ↗
  • MalfunctionJun 28, 2021Explosion

    IT WAS REPORTED THAT DURING A PROCEDURE, UPON ANCHOR INSERTION, BOTH ANCHORS EXPLODED/SHATTERED ON THE FIRST TAP WITH HAMMER. THE CORRECT DRILL AND DETAILS WERE USED PERFORMING THE INSERTION OF ANCHORS ACCORDING TO MANUEL/TECHNIQUE GUIDES. THE CASE WAS COMPLETED BY USING A NEW AR-2924BCH.

    Patient problems: Insufficient Information

    MAUDE report 12076185 ↗
  • MalfunctionMay 10, 2021Break

    IT WAS REPORTED THAT DURING A PROCEDURE, THE SURGEON WAS USING THE BIO 2.4 MINI HIP PUSHLOCKS AND THE ANCHORS BROKE UPON USING. BOTH SHATTERED ON THE FIRST TAP WITH HAMMER. THE CORRECT DRILL AND DETAILS WERE USED PERFORMING THE INSERTION OF ANCHORS ACCORDING TO MANUEL/TECHNIQUE GUIDES. THE CASE WAS COMPLETED BY USING A NEW AR-2924BCH AND AR-2924DH-2.

    Patient problems: Insufficient Information

    MAUDE report 11799051 ↗

Other Fastener, fixation, biodegradable, soft tissue devices

All Fastener, fixation, biodegradable, soft tissue devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page