VOLT 02.527.069Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982337528), received between Aug 8, 2025 and Feb 20, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 20, 2026Device-Device Incompatibility

  IT WAS REPORTED THAT SURGEON WAS TREATING A DISTAL HUMERUS FRACTURE SHOWN BELOW AND A 2.7MM VOLT LOCKING SCREW, 16MM DID NOT LOCK INTO ONE OF THE TWO HEAD HOLES OF 2.7MM VOLT CONDYLAR PLATE. ACCORDING TO SURGEON PREDRILL 2.0MM HOLE WITH SPHERICAL TIP OF DRILL GUIDE IN THE POSTERIOR LATERAL COLUMN OF DISTAL HUMERUS AND 2.7MM VOLT LOCKING SCREW, 16MM DID NOT LOCK INTO ONE OF THE HEAD HOLES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24402109 ↗
• MalfunctionAug 8, 2025Device-Device Incompatibility; Device-Device Incompatibility

  THE FOLLOWING PRODUCT ISSUES WERE REPORTED TO HAVE OCCURRED ON AN UNKNOWN DATE: DEPTH GAUGE FOR 3.5MM CORTEX SCREWS (X 3) - HOOK IS BROKEN FROM USAGE IN PELVIS. RATCHET WRENCH-11MM WIDTH ACROSS FLATS (X 3) - RATCHET DOESN'T WORK. 2.4/2.7 VOLT(TM) SCR RACK 6-90 2 HIGH 1/3 WIDTH ALUM FRAME (X 2) - RACKS ARE FADED FROM WASH AND SOAP. 1 .6MM/0.8MM DOUBLE DRILL GUIDE (X 2) - GUIDE IS BENT. 2. 0MM/1.1MM DOUBLE DRILL GUIDE (X 2) - GUIDE IS BENT. 2.7MM COMPRESSION/DISTRACTION POST/FOR VA-LOCKING HOLE X 6- THREADS ARE STRIPPED. 2.8MM GUIDE WIRE/ 300MM LENGTH FLUTED TIP (X 6)- THREADS STRIPPED. 2.7MM VOLT(TM) CONDYLAR PLATE 6H/58MM (X 1) - PLATE DID NOT LOCK WITH LOCKING SCREW. 2.7MM VOLT(TM) CONDYLAR PLATE 10H/95MM (X 1) PLATE DID NOT LOCK WITH LOCKING SCREW. 15.5MM MONOBLOC FLEXIBLE REAMER - LONG (X 2) - REAMERS ARE DULL. PERIOSTEAL ELEVATOR 14MM STRAIGHT BLADE-ROUND EDGE (X 3)- RUST ON ELEVATOR. THERE WAS NO PATIENT INVOLVEMENT; ISSUES WERE NOTED IN STERILE PROCESSING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22748423 ↗