RESTORE 219341Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10886705005864), received between Apr 1, 2020 and Feb 10, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 10, 2025Degraded; Dull, Blunt; Degraded; Dull, Blunt

  IT WAS REPORTED THAT WHILE PERFORMING AN ANTERIOR CRUCIATE LIGAMENT TECHNIQUE, DURING THE BROCADE OF THE TIBIA, A DRILL BIT DEVICE OF TIBIA WAS USED WITH THE RESTORE FULLFLUTE REAM DEVICE WHICH WAS INEFFICIENT AND THE ASSISTANT SPECIALIST HAD TO EXERT MORE FORCE TO PERFORM THE TUNNEL AND IN TURN. A LOT OF DELAY OCCURRED DURING THIS STEP, THE STATE OF THE MOTOR AND BATTERY WERE VERIFIED TO RULE OUT FAILURES OF THE POWER EQUIPMENT. SATISFACTORY TO THE ASSESSMENT IN TERMS OF FORCE AND SPEED, THIS BEING RULED OUT AS CAUSAL. THE PROCESS TAKES LONGER THAN USUAL TO CROSS THE METAPHYSIS AND EFFECTIVELY PERFORATE THE ARTICULAR CORTEX OF THE TUNNEL, THE TIP OF THE BUTTONHOLE PIN WAS PROTECTED WITH A CURETTE, HOWEVER, THE FORCE ADMINISTERED TO BE ABLE TO PIERCE THE ARTICULAR CORTEX MUST BE SO MUCH THAT AT THE EXIT OF THE JOINT. IT WAS IMPOSSIBLE TO CONTROL THAT THE DRILL BIT WAS NOT AT THE END OF THE JOINT. THIS IS REPORT 2 OF 2 OF (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21348814 ↗
• MalfunctionFeb 16, 2023Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

  THIS IS REPORT 6 OF 15 FOR (B)(4). IT WAS REPORTED BY THE FIELD SERVICE ENGINEER THAT DURING INSPECTION, THE CUSTOMER OBSERVED THAT THE RESTORE FULLY FLUTED REAMER 11MM, 40-130MM (PLUS OR MINUS 5 PERCENT) DEVICE HAD CONTAMINATION INSIDE ITS CANNULATED SECTION. ACCORDING TO THE REPORT, THE EVENT OCCURRED BEFORE PROCESSING WHEN THE CUSTOMER DECIDED TO INSPECT THE DEVICE WITH THEIR BORESCOPE. IT WAS REPORTED THAT THE DEVICE WAS PURCHASED ON JUNE 2022; AND HAS NEVER BEEN USED. IT WAS FURTHER REPORTED THAT THE DEVICE WAS SHELVED AND STORED IN CONTROLLED ENVIRONMENT IN THE STERILE PROCESSING DEPARTMENT. THERE WAS NO PROCEDURE NOR PATIENT INVOLVEMENT REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16386081 ↗
• MalfunctionApr 1, 2020Dull, Blunt; Dull, Blunt

  IT WAS REPORTED BY SALES REP VIA PHONE THAT BEFORE AN ACL PROCEDURE THE PHYSICIAN NOTICED THAT THE SIZE OF THIS CRUCIATE + RETROREAMER BULLET WAS TOO BIG AND WOULDN´T FIT. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. NO PATIENT CONSEQUENCES OR SURGICAL DELAY REPORTED. AFTER THE PROCEDURE WAS FINISHED THE REP INSPECTED HIS PRODUCTS AND NOTICED THAT THE FOLLOWING DEVICES WERE DULL: FULLY FLUTED REAMER (6 MM, 6.5 MM, 7 MM, 7.5 MM, 8 MM, 8.5 MM, 9 MM, 9.5 MM, 10 MM, 10.5 MM, 11 MM, 11.5 MM, 12 MM). ALL DEVICES ARE AVAILABLE TO BE RETURNED FOR EVALUATION. THIS COMPLAINT IS RELATED TO (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9913756 ↗