Arthrex® AR-9142-17PRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867057678), received between Oct 30, 2020 and Oct 30, 2020 — classified as 1 injury.

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

• InjuryOct 30, 2020Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THROUGH THE SURGICAL OUTCOME SYSTEM THAT A PATIENT MAY HAVE HAD AN ISSUE AS A RESULT OF SURGERY INVOLVING ARTHREX IMPLANTS. UPON FURTHER INVESTIGATION IT WAS DISCOVERED THAT A PATIENT HAD A (B)(6) 2018 TOTAL SHOULDER ARTHROPLASTY PROCEDURE. (B)(6) 2018, A FEW DAYS POST SURGERY, THE PATIENT WAS EXPERIENCING INABILITY TO EXTEND FINGERS. THE PATIENT WAS DIAGNOSED WITH RADIAL NERVE PALSY. PATIENT WAS ABLE TO EXTEND WRIST ON (B)(6) 2019 BUT HAD DIFFICULTY TYPING. AN EMG WAS RECOMMENDED. PATIENT WAS TOLD NERVE PALSY WOULD RESOLVE WITHIN THE YEAR. THE PATIENT CONSULTED WITH AN ORTHOPEDIC HAND SURGERY SPECIALIST WHO SUGGESTED A TENDON TRANSFER FOR THE NERVE PALSY. IT IS UNKNOWN IF THE PATIENT HAS PROCEEDED WITH A SECOND SURGERY WITH ANOTHER SURGEON. THE PATIENT HAS HAD NO FURTHER SURGERIES WITH THE ORIGINAL SURGEON. THE FOLLOWING ARE THE ARTHREX PRODUCTS THAT WERE IMPLANTED (B)(6) 2018: AR-9100-06S / LOT: 10233337, AR-9106-01 / LOT: 1027261806, AR-9142-17P / LOT: 170097421.

  Patient problems: Dyskinesia; Nerve Damage

  MAUDE report 10763968 ↗