BD Micro-Fine 329410Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 30382903294108), received between Oct 3, 2019 and Nov 12, 2020 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 12, 2020Break; Leak/Splash; Break; Leak/Splash

  IT WAS REPORTED THAT 5 SYRINGE 1.0ML 28GA 1/2IN 10BAG 500 BDD WERE DAMAGED BEFORE USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT THE SYRINGES WERE DAMAGED. VERBATIM: HELLO, I NEED TO REPORT A DAMAGED & REFUSED ON A RECENT PO."

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10831824 ↗
• MalfunctionJul 29, 2020Failure to Deliver; Failure to Deliver

  IT WAS REPORTED THAT SYRINGE 1.0ML 28GA 1/2IN 10BAG 500 BDD WAS UNABLE TO DRAW UP INSULIN DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 329410 BATCH NO. 0034135. IT WAS REPORTED THAT SHE IS UNABLE TO DRAW UP INSULIN IN SOME SYRINGES. SOMETIMES THE NEEDLES ARE CLOGGED AND NOT RELEASE INSULIN ONCE IT'S DRAWN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10341934 ↗
• MalfunctionMay 1, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THE BOX LABEL INFORMATION IS MISSING WITH A BD 1ML ULTRA FINE¿ INSULIN SYRINGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT THERE IS NO EXPIRATION DATE OR COPYRIGHT DATE ON ANY OF THE BOXES.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10019324 ↗
• MalfunctionOct 3, 2019Leak/Splash; Delivered as Unsterile Product; Defective Device; Leak/Splash; Delivered as Unsterile Product; Defective Device

  IT WAS REPORTED THAT SYRINGE 1.0ML 28GA 1/2IN 10BAG 500 BDD WAS DAMAGED. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 329410 BATCH NO: 7100965. IT WAS REPORTED PLUNGER ROD BENT, SEPARATED FROM RUBBER STOPPER, PLUNGER CAP LOOSE INSIDE OF BAG.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9153099 ↗