Arthrex® AR-7000-30Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867040984), received between Dec 14, 2016 and Dec 14, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Bent” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 14, 2016Bent

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT LATERJET PROCEDURE ON 06/7/16, WHERE A 3.75X32MM CANNULATED PARTIALLY THREADED SCREW (AR-7000-32, LOT: 1457740, (B)(4) (B)(6)) WAS IMPLANTED ALONG WITH A 3.75X30MM CANNULATED PARTIALLY THREADED SCREW (AR-7000-30, LOT: 1457565, (B)(4) (B)(6)). ON AN UNKNOWN DATE, THE PATIENT SUFFERED FROM A SEIZURE CAUSING THE AR-7000-32 TO BEND. A REVISION SURGERY TOOK PLACE ON (B)(6) 2016 AND THE PATIENT HAD THE AR-7000-32, LOT: 1457740, EXPLANTED AND REPLACED WITH AN AR-7000-34, LOT: 1457742. THE AR-7000-30, LOT: 1457565, WAS ALSO EXPLANTED AND REPLACED WITH AN AR-7000-32, LOT: 10034143. PATIENT IS A (B)(6) FEMALE. NO PATIENT INJURY.

  Patient problems: Seizures

  MAUDE report 6173242 ↗