Arthrex® AR-300PD24Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888867100176), received between Mar 28, 2024 and Sep 16, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 16, 2026Positioning Failure; Use of Device Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50787474 ↗
• MalfunctionApr 28, 2025Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT DURING A MICA SURGERY THE DEVICE DID NOT GRIP THE 2.4 K WIRES PROPERLY. PER COMPLAINT REPORTER THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A NEW DEVICE FROM STRYKER. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21919940 ↗
• MalfunctionMay 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A MICA SURGERY THE ATTACHMENT DOES NOT HOLD THE WIRE FIRMLY AND SLIPS. THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY REPORTED. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A NEW DEVICE WITH THE SAME PART NUMBER. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19388063 ↗
• MalfunctionMay 23, 2024Break; Break

  IT WAS REPORTED THAT DURING A SURGERY A BOLT OF THE DEVICE FOR SECURING THE LOCK HAS FALLEN OUT. AS A RESULT, THE WIRE IS NO LONGER STUCK IN THE HOLDER. ACCORDING TO THE SURGEON NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY OCCURRED. THE SURGERY WAS FINISHED SUCCESSFULLY. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY. UPDATE AVOE 28-APR-2023: IT WAS CONFIRMED THAT THE BOLT FELL OUT DURING A MICA (MINIMALLY INVASIVE CHEVRON AND AKIN) SURGERY. THE SURGERY WAS FINISHED SUCCESSFULLY BY INSERTING K-WIRES WITH A SMALLER DIAMETER AND CONTINUING THE DRILLING PROCESS. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19387830 ↗
• MalfunctionMar 28, 2024Defective Device; Defective Device

  IT WAS REPORTED THAT THE LOCKING MECHANISM FOR THE WIRES IS TOO WEAK. THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY REPORTED. THERE WAS NO CASE INVOLVEMENT REPORTED. NO FURTHER INFORMATION RECEIVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18995122 ↗