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N/A 301692Recalls & reported problems

Becton, Dickinson And Company · NEEDLE 16GA 3/4IN BLT SQ · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 30382903016922), received between Oct 9, 2023 and Oct 16, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Defective Component” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K021475); they may or may not involve this specific model.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Defective Component1
  • Packaging Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 16, 2023Defective Component; Defective Component

    IT WAS REPORTED THAT THE BLUNT FILL NEEDLE PRECISIONGLIDE¿ HAS A NEEDLE DEFECT. THE FOLLOWING WAS RECEIVED BY THE INITIAL REPORTER: WE HAVE COME ACROSS AN ISSUE WITH A LOT OF NEEDLES THAT WE PURCHASED FROM BECTON DICKINSON. IT HAS BEEN BROUGHT TO OUR ATTENTION THAT A NUMBER OF THESE NEEDLES DID NOT HAVE BLUNTED TIPS, BUT RATHER FLAT SHARP END

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17946859 ↗
  • MalfunctionOct 9, 2023Packaging Problem; Packaging Problem

    IT WAS REPORTED THAT THE BD BLUNT FILL NEEDLE HAD MIX PRODUCT IN PACK. THE FOLLOWING WAS TRANSLATED FROM GERMAN TO ENGLISH: THE PRODUCT IS A BLUNT NEEDLE, IT IS SO THAT POINTED NEEDLES HAVE BEEN FOUND IN THE BATCH MENTIONED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17896049 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K021475. One submission often covers many models, so check the product and lot details in each record.

  • Z-0588-2021 · Nov 18, 2020 · Terminated
    BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the bo
  • Z-0207-2018 · May 31, 2017 · Terminated
    BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain bl
  • Z-1009-2012 · Oct 8, 2011 · Terminated
    BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications

Other Needle, hypodermic, single lumen devices

All Needle, hypodermic, single lumen devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page