Insulin Syringes, 1mL 30G x 8MM 328505Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00681131311687), received between Jan 31, 2018 and Jun 2, 2020 — classified as 2 malfunctions.

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

• MalfunctionJun 2, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 1.0ML 30GA 8MM 10ABAG 500 WAL WAS MISSING AN EXPIRATION DATE FROM THE SHELF CARTON. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT EXPIRATION DATE IS MISSING FROM BOX. VERBATIM: BD MAIL FULFILLMENT HAS SEVERAL BOXES WITHOUT EXP DATE INFO ON THE BOXES. INFORMED FULFILLMENT TO DESTROY THE BOXES AND NOT SEND THEM OUT TO THE CONSUMERS FOR REPLACEMENT."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10107577 ↗
• MalfunctionJan 31, 2018Detachment Of Device Component

  IT WAS REPORTED THAT TWO OF THE BD RELION¿ INSULIN SYRINGES HAD SHIELDS MISSING AND WERE LYING ON THE BOTTOM OF THE BAG. FOUND BEFORE USE. NO SERIOUS INJURY OR MEDICAL INTERVENTION NOTED.

  Patient problems: No Information

  MAUDE report 7232651 ↗