Arthrex® AR-8150PP-30Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867042902), received between May 3, 2024 and May 14, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Activation Failure” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 14, 2024Defective Device; Defective Device

  IT WAS REPORTED ON 07/01/2022 BY A FACILITY REPRESENTATIVE VIA (B)(4) THAT AN AR-8150PP-30 POWERPICK LEVER WAS STUCK AND NEEDLE WAS JAMMED. THIS WAS DISCOVERED DURING A CASE WITH NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19311072 ↗
• MalfunctionMay 3, 2024Activation Failure; Activation Failure

  IT WAS REPORTED THAT UPON OPENING THE AR-8150PP-30 POWER PICK TO THE FIELD, IT WAS BEING CHECKED TO MAKE SURE THE LEVER TO DEPLOY THE PICK PART OF THE INSTRUMENT WORKED, BUT WHEN THE LEVER WAS ACTIVATED THE PICK DID NOT DEPLOY COMPLETELY. A SECOND PICK FROM THE SAME BOX WAS OPENED AND USED TO COMPLETE THE PROCEDURE.

  Patient problems: Insufficient Information

  MAUDE report 19243305 ↗