GLASS VAN #312Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 18904233119999), received between Oct 6, 2025 and Oct 6, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjuryOct 6, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT DURING THE RIGHT XLIF PROCEDURE A FOREIGN OBJECT WAS NOTED ON X-RAY AFTER TEMPLATING OF INTERBODY CAGE. WAS DETERMINED TO BE A BLADE THAT HAD BEEN EXTRACTED FROM INSTRUMENT AND REMAINED IN L2-3 LEVEL. A DETERMINATION WAS MADE TO REMOVE THE BLADE OBJECT IN DOING A LEFT DIRECT APPROACH PROCEDURE TO REMOVE OBJECT WHICH CREATED A SECONDARY PROCEDURE, AND STAGING OF CASE FOR A LATER DATE. THE OBJECT WAS DETERMINED TO BE A MYCO MEDICAL GLASS VAN CS SURGICAL BLADE. THE REF #01999, LOT #210311MC, EXPIRES: 11-22-2026, MYCO REORDER #(B)(4). MYCO MEDICAL PHONE # (B)(6). THE OBJECT WAS REMOVED AND VERIFIED WITH X-RAY THAT NO OTHER FRAGMENTS WERE INTACT WITHIN LEFT L4-L5 LEVEL OF REMOVING THE OBJECT.

  Patient problems: Foreign Body In Patient

  MAUDE report 23222516 ↗