BD Integra 305275Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903052752), received between Oct 17, 2019 and Jun 30, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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. How this data works · Data updated Oct 13, 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 30, 2021Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT NEEDLE INTEGRA 18X1-1/2 BLUNT FILL EXPERIENCED A CASE OF THE SYRINGE AND MATING COMPONENT SEPARATING, AND THE TIP/LUER OF SYRINGE BREAKING OFF. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: LATELY, THE NURSES ARE EXPERIENCE LOW SUCTION, AND LOSS OF AIR WHEN PLUNGED INTO THE VIAL. ALSO IT DOES NOT SEEM TO THREAD SECURELY TO THE SYRINGE AND WILL SNAP OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12095119 ↗
• MalfunctionOct 17, 2019Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT RUBBER-LIKE FOREIGN MATTER WAS NOTICED FLOATING IN THE NEEDLE INTEGRA 18X1-1/2 BLUNT FILL DURING USE AFTER DRAWING UP MEDICATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "AFTER DRAWING UP MEDICATION USING THE BD BLUNT FILL NEEDLE (WITHOUT FILTER) THE NURSE NOTICED "FLOATER IN THE MEDICATION SYRINGE". SHE DESCRIBED IT AS RESEMBLING A SMALL AMOUNT OF RUBBER."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9203272 ↗