Medline Industries, Inc. SPEC0070Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884389517918), received between Nov 9, 2018 and Nov 9, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Crack” (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 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.

• MalfunctionNov 9, 2018Crack

  MD WAS BEGINNING THE SET UP OF A PATIENT'S SHOULDER INJECTION WHEN SHE NOTICED THAT THE SYRINGE USED TO DRAW UP LIDOCAINE WAS CRACKED. THE SAME MD HAD THE SAME THING HAPPEN A WEEK PRIOR WHILE SETTING UP ANOTHER PROCEDURE. ANOTHER MD AT A NEARBY FACILITY ALSO HAD THIS HAPPEN TO HER WITH THE SAME KIT. THE CRACK WAS NOT IDENTIFIED IN THIS INSTANCE AND THE LIDOCAINE SHOT ACROSS THE ROOM. IN THIS EVENT, THE REPORTER OF THIS EVENT HAS SPOKEN TO THE VENDOR AND THE VENDOR CAME TO PICK UP THE SYRINGE AND TO TAKE A LOOK AT IT LAST WEEK.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8054665 ↗