N/A 305155Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00382903051557), received between Sep 14, 2018 and Jul 17, 2024 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 17, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem

  MATERIALS#: 305155. BATCH#: 1300351. IT WAS REPORTED BY THE CUSTOMER THAT CUSTOMER WHO DOES WEEKLY INJECTION NOTICED THAT THERE WAS 3 OF ITEM 305196 LOT 1120197 AND 2 OF ITEM 305196 LOT -2327243 WITHIN THE BOX OF 100 COUNT ITEM 305155.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19762464 ↗
• MalfunctionApr 13, 2023Loose or Intermittent Connection; Loose or Intermittent Connection

  IT WAS REPORTED THAT THE BD PRECISIONGLIDE¿ NEEDLE PULLED OUT OF THE HUB WHEN TRYING TO REMOVE THE NEEDLE FROM THE SYRINGE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 1ST OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "HAPPENED TWICE- WHEN TRY TO CAP AND REMOVE THE NEEDLE OFF SYRINGE THE METAL NEEDLE COMES BUT GRAY PLASTIC REMAINS ON THE SYRINGE (HUB) BREAKS AWAY FROM THE NEEDLE ( WHEN TRYING TO REMOVE THE NEEDLE FROM SYRINGE )".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16740465 ↗
• MalfunctionApr 12, 2023Loose or Intermittent Connection; Loose or Intermittent Connection

  IT WAS REPORTED THAT THE BD PRECISIONGLIDE¿ NEEDLE PULLED OUT OF THE HUB WHEN TRYING TO REMOVE THE NEEDLE FROM THE SYRINGE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 2ND OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "ISSUE : HAPPENED TWICE- WHEN TRY TO CAP AND REMOVE THE NEEDLE OFF SYRINGE THE METAL NEEDLE COMES BUT GRAY PLASTIC REMAINS ON THE SYRINGE (HUB) BREAKS AWAY FROM THE NEEDLE ( WHEN TRYING TO REMOVE THE NEEDLE FROM SYRINGE )".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16729094 ↗
• MalfunctionMar 22, 2021Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE NEEDLE 22X1 RB PULLED OUT OF THE HUB WHILE INJECTING A DOG AND REMAINED BETWEEN THE SHOULDER BLADES. THE NEEDLE WAS ABLE TO BE REMOVED BY HAND FROM THE PATIENTS BODY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE MEDICATION WAS DRAWN UP WITH A DIFFERENT NEEDLE. THIS NEEDLE WAS PLACED ONTO THE SYRINGE AND GAVE A SUBCUTANEOUS INJECTION TO A SMALL DOG BETWEEN THE SHOULDER BLADES. THE DOG WAS VERY STILL AND AS THE NEEDLE WAS PULLED OUT IT WAS NOTICED THAT THE NEEDLE WAS NO LONGER ON THE HUB. LOOKED AT THE PATIENT AND THE NEEDLE WAS SLIGHTLY STICKING OUR AND WAS ABLE TO PULL IT OUT OF THE PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11548394 ↗
• MalfunctionMar 4, 2021Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT A NEEDLE 22X1 RB HAD FOREIGN MATTER DURING USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT THERE IS A SMALL STYROFOAM BALL IN THE BEVEL TIP. VERBATIM: PER CUSTOMER'S RESPONSE: (B)(6) 2021. EVENT DATE (B)(6) 2021. NO ONE HURT. OPENED A NEW BD PRECISIONGLIDE NEEDLE 22G X 1 LOT# 9162963 AND WHEN UNCAPPING THE NEEDLE FOUND WHAT APPEARS TO BE A SMALL STYROFOAM BALL IN THE BEVEL TIP."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11417969 ↗
• MalfunctionFeb 18, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS NO EXPIRATION DATE LISTED ON THE NEEDLE 22X1 RB BOX. THIS COMPLAINT WAS CREATED TO CAPTURE THE 3RD OF 3 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PHARMACIST STATED, BOXES DON'T HAVE AN EXPIRATION DATE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 11346359 ↗
• MalfunctionMar 19, 2019Break; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING USE OF THE BD PRECISIONGLIDE NEEDLE THAT SYRINGE NEEDLE BROKE OFF OF SYRINGE WHILE DRAWING AND WAS STUCK IN THE VIAL. THE NEEDLE BROKE OFF IN CONSUMERS LEG AND IN THE VIAL. FROM PHONE CALL ON (B)(6) 2019 16:06:07: CONSUMER CALLED, I UPDATED THE CONTACT INFORMATION. PROBLEM OCCURRED ABOUT 3 WEEKS AGO. CONSUMER ALSO STATED THAT ONE NEEDLE BROKE OFF IN HIS LEG DURING INJECTION, HE REMOVED IT WITH HIS FINGERS, NO MEDICAL INTERVENTION, NO INJURY. SAMPLES WERE DISCARDED, SENDING REPLACEMENT BOX TO THE PHARMACY. PHARMACIST REPORTED ON BEHALF OF CONSUMER THAT SYRINGE NEEDLE BROKE OFF OF SYRINGE WHILE DRAWING AND WAS STUCK IN THE VIAL. OCCURRENCE DATE IS UNKNOWN, LOT # 5336578, PRODUCT # 305155, EXP 1-31-2021.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8433301 ↗
• MalfunctionSep 14, 2018Contamination /Decontamination Problem

  IT WAS REPORTED WITH THE USE OF THE BD PRECISIONGLIDE¿ NEEDLE THERE WAS AN ISSUE WITH FOREIGN MATTER. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7877674 ↗

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