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BD Luer-Lok 305617Recalls & reported problems

Becton, Dickinson And Company · SYRINGE 20ML LL TIP CONV PAK · Class 2

Quick summary

This BD Luer-Lok syringe is a 20 mL piston syringe. Reports mostly describe leaks and contamination, including particles and silicone lubricant in shipments, along with occasional breaks and labeling issues. There are 90 reports, no deaths, and no injuries. No recalls name this device.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
90
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 90 adverse event reports that list this exact device (DI 00382903056170), received between Nov 27, 2017 and Jun 17, 2026 — classified as 90 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (36 reports).

10 other recalls cover devices cleared under the same FDA submission (K110771); 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: 1 reportsDec 2023: 0 reportsJan 2024: 1 reportsFeb 2024: 1 reportsMar 2024: 1 reportsApr 2024: 1 reportsMay 2024: 1 reportsJun 2024: 1 reportsJul 2024: 1 reportsAug 2024: 1 reportsSep 2024: 3 reportsOct 2024: 1 reportsNov 2024: 1 reportsDec 2024: 3 reportsJan 2025: 1 reportsFeb 2025: 2 reportsMar 2025: 1 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 2 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 1 reportsDec 2025: 3 reportsJan 2026: 2 reportsFeb 2026: 5 reportsMar 2026: 4 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520265
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Leak/Splash36
  • Device Contamination with Chemical or Other Material26
  • Contamination /Decontamination Problem10
  • Device Markings/Labelling Problem8
  • Break4
  • Contamination4
  • Crack3
  • Volume Accuracy Problem3

Patient problems

  • No Clinical Signs, Symptoms or Conditions58
  • No Known Impact Or Consequence To Patient20
  • No Consequences Or Impact To Patient8
  • No Information2
  • No Patient Involvement2

Recent adverse event reports

The 25 most recent of 90 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 17, 2026Contamination /Decontamination Problem

    IT WAS REPORTED BY THE CUSTOMER THAT DURING THE CHARACTERIZATION, IT TRACED BACK TO A MATERIAL, A PARTICLE WAS CONSISTENT WITH POLYSOME AND BUTADIENE. THEY USED IN TOTAL 80 SYRINGES (8 PACKS OF 10), THEY ONLY DISCOVERED IT IN 2 OF THEM BUT DON'T KNOW THE LOT NUMBER OF THE SPECIFIC ONES WITH THAT PARTICLE. VERBATIM: COMPLAINT VIA PHONE. CASE DESCRIPTION: THE SYRINGE WAS USED FOR A RECONSTITUTION, A PROCEDURE THEY PERFORM. DURING THE CHARACTERIZATION, IT TRACED BACK TO A MATERIAL, A PARTICLE WAS CONSISTENT WITH POLYSOME AND BUTADIENE. THEY USED IN TOTAL 80 SYRINGES (8 PACKS OF 10), THEY ONLY DISCOVERED IT IN 2 OF THEM BUT DON'T KNOW THE LOT NUMBER OF THE SPECIFIC ONES WITH THAT PARTICLE. THE CUSTOMER CALLED TO KNOW WHAT'S THE COMPOSITION OF THE SYRINGE AND WAS TRANSFERRED TO MED INFO, WHERE THEY REACHED THE ENGINEERING TEAM AND ARE GONNA CONTACT HER WITH THE INFORMATION. ADDITIONAL INFORMATION RECEIVED ON 5-JUN-2026: 1. CAN YOU PLEASE PROVIDE AN EXACT DATE OF EVENT IN FORMAT DD-MMM-YYYY? THE PARTICULATE WAS CHARACTERIZED (FTIR) AND REPORTED ON (B)(6) 2026 AS CONSISTENT WITH POLYSTYRENE POSSIBLY WITH A SMALL AMOUNT OF BUTADIENE. 2. CAN YOU SHARE ANY PHYSICAL SAMPLE OR PHOTO IF AVAILAB

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25535312 ↗
  • MalfunctionMar 23, 2026Contamination /Decontamination Problem

    IT WAS REPORTED BY CUSTOMER THAT HAD 28 UNITS REJECTED FOR SUSPECTED PARTICULATES. VERBATIM: COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED DMR # 671 PO #: (B)(6)_DEFECT MATERIAL DESCRIPTION: SYRINGE TRAY, 20ML BD 10PK (REF. 305617) LOT NUMBER: 5181420 ITEM CODE: 305617 DEFECTIVE QUANTITY: 28 DEFECT DESCRIPTION: SYRINGE LOT (5181420) AND HAD28 UNITS REJECTED FOR SUSPECTED PARTICULATES. OBSERVED DATE: JANUARY 30, 2026 OBSERVED DURING WHICH PROCESS STAGE: COMPOUNDING IR/ DMI NUMBER IF LAUNCHED: DEV-04261 SAMPLE AVAILABILITY FOR SUPPLIER TO INVESTIGATE: NO IS DEFECTIVE EVIDENCE (I.E. PICTURES; TEST RESULTS ETC.) AVAILABLE? YES IS PATIENT IMPACTED? NO IF DEFECT HAS BEEN REPORTED TO THIRD PARTY? NO IF THE DEFECT REPORT FROM XXX CUSTOMER? NO IS THERE A TREND OBSERVED? NO SUPPLIER ACTION AWARENESS/ ATTENTION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24663545 ↗
  • MalfunctionMar 13, 2026Break

    IT WAS REPORTED BY THE CUSTOMER THAT ONE INCIDENT LEADING TO PATIENT ADVERSE REACTION. IN THE FIRST INCIDENT, A GROUP OF SYRINGES BROKE AT THE PHALANGE WHILE BEING STORED IN A FREEZER WITH RECONSTITUTED CEFEPIME 2 G IN 20 ML STERILE WATER. IN THE SECOND INCIDENT, A SYRINGE TIP BROKE OFF IN AN IV INFUSION LINE Y-SITE AFTER ADMINISTRATION OF CEFEPIME 2 G IN 20 ML STERILE WATER. RCC RECEIVED A COMPLAINT VIA WEB. PIR ATTACHED. THERE HAVE BEEN TWO INCIDENTS AT MY INSTITUTION XXXXXXXXXX) WHERE THESE 20 ML LUER LOCK SYRINGES BROKE, WITH ONE INCIDENT LEADING TO PATIENT ADVERSE REACTION. IN THE FIRST INCIDENT, A GROUP OF SYRINGES BROKE AT THE PHALANGE WHILE BEING STORED IN A FREEZER WITH RECONSTITUTED CEFEPIME 2 G IN 20 ML STERILE WATER. IN THE SECOND INCIDENT, A SYRINGE TIP BROKE OFF IN AN IV INFUSION LINE Y-SITE AFTER ADMINISTRATION OF CEFEPIME 2 G IN 20 ML STERILE WATER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24597967 ↗
  • MalfunctionMar 13, 2026Contamination /Decontamination Problem

    IT WAS REPORTED BY CUSTOMER THAT BD 20ML SYRINGE LOT 5181420, IR SPECTRUM DEMONSTRATED A 79.2 MATCH TO SILICONE LUBRICANT AND, WHEN COMPARED TO THE BROADER FTIR LIBRARY, A 93.7 MATCH TO SILASTIC Q7 4550, A PEROXIDE CURED MEDICAL GRADE SILICONE ELASTOMER CONSISTENT WITH STOPPER CONSTRUCTION. RCC RECEIVED A COMPLAINT VIA EMAIL. DMR # (B)(4) PO #: (B)(4) DEFECT MATERIAL DESCRIPTION: SYRINGE TRAY, 20ML BD 10PK (REF. 305617) LOT NUMBER: 5181420 ITEM CODE: 305617 DEFECTIVE QUANTITIES: 1 DEFECT DESCRIPTION: BD 20ML SYRINGE LOT 5181420, IR SPECTRUM DEMONSTRATED A 79.2 MATCH TO SILICONE LUBRICANT AND, WHEN COMPARED TO THE BROADER FTIR LIBRARY, A 93.7 MATCH TO SILASTIC Q7 4550, A PEROXIDE CURED MEDICAL GRADE SILICONE ELASTOMER CONSISTENT WITH STOPPER CONSTRUCTION. NO UNITS ARE AVAILABLE TO BE RETURNED. OBSERVED DATE: (B)(6) 2026 OBSERVED DURING WHICH PROCESS STAGE: ILP IR/ DMI NUMBER IF LAUNCHED: DEV-04209 SAMPLE AVAILABILITY FOR SUPPLIER TO INVESTIGATE: NO IS DEFECTIVE EVIDENCE (I.E. PICTURES; TEST RESULTS ETC.) AVAILABLE? YES, IS PATIENT IMPACTED? NO IF DEFECT HAS BEEN REPORTED TO THIRD PARTY? NO IF THE DEFECT REPORT FROM QUVA CUSTOMER? NO IS THERE A TREND OBSERVED? NO".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24597965 ↗
  • MalfunctionMar 13, 2026Break

    IT WAS REPORTED BY THE CUSTOMER THAT ONE INCIDENT LEADING TO PATIENT ADVERSE REACTION. IN THE FIRST INCIDENT, A GROUP OF SYRINGES BROKE AT THE PHALANGE WHILE BEING STORED IN A FREEZER WITH RECONSTITUTED CEFEPIME 2 G IN 20 ML STERILE WATER. IN THE SECOND INCIDENT, A SYRINGE TIP BROKE OFF IN AN IV INFUSION LINE Y-SITE AFTER ADMINISTRATION OF CEFEPIME 2 G IN 20 ML STERILE WATER. RCC RECEIVED A COMPLAINT VIA WEB. PIR ATTACHED. THERE HAVE BEEN TWO INCIDENTS AT MY INSTITUTION XXXXXXXXXX) WHERE THESE 20 ML LUER LOCK SYRINGES BROKE, WITH ONE INCIDENT LEADING TO PATIENT ADVERSE REACTION. IN THE FIRST INCIDENT, A GROUP OF SYRINGES BROKE AT THE PHALANGE WHILE BEING STORED IN A FREEZER WITH RECONSTITUTED CEFEPIME 2 G IN 20 ML STERILE WATER. IN THE SECOND INCIDENT, A SYRINGE TIP BROKE OFF IN AN IV INFUSION LINE Y-SITE AFTER ADMINISTRATION OF CEFEPIME 2 G IN 20 ML STERILE WATER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24594480 ↗
  • MalfunctionFeb 13, 2026Contamination

    IT WAS REPORTED BY CUSTOMER THAT THEY CONFIRMED SILICONE OIL PRESENCE ASSOCIATED WITH THE SUPPLIED COMPONENT LOT. RCC RECEIVED A COMPLAINT VIA EMAIL. DMR # (B)(4) PO #: (B)(4) DEFECT MATERIAL DESCRIPTION: SYRINGE TRAY, 20ML BD 10PK (REF. 305617) LOT NUMBER: 5195502, 5181420, ITEM CODE: 305617, DEFECTIVE QUANTITY: 2 , DEFECT DESCRIPTION: THIS DMR IS INITIATED TO FORMALLY NOTIFY THE SYRINGE SUPPLIER OF CONFIRMED (B)(4) WITH THE SUPPLIED COMPONENT LOT, IDENTIFIED DURING INTERNAL QUALITY INVESTIGATION. ALTHOUGH NO PARTICULATE MATTER WAS CONFIRMED BY FTIR ANALYSIS OR QC VISUAL ASSESSMENT, THE INVESTIGATION CONCLUDED THE OBSERVED DEFECT WAS SILICONE OIL. WE WISH TO REQUEST FOR SILICON OIL ADDITION SPECIFICATION AND THE SAFETY JUSTIFICATION REPORT/DATA (MEDICAL GRADE/ INERT, BIOCOMPATIBLE, ETC) OBSERVED DATE: (B)(6) 2026 OBSERVED DURING WHICH PROCESS STAGE: ILP IR/ DMI NUMBER IF LAUNCHED: (B)(4) SAMPLE AVAILABILITY FOR SUPPLIER TO INVESTIGATE: NO IS DEFECTIVE EVIDENCE (I.E. PICTURES; TEST RESULTS ETC.) AVAILABLE? YES, IS PATIENT IMPACTED? NO, IF DEFECT HAS BEEN REPORTED TO THIRD PARTY? NO , IF THE DEFECT REPORT FROM QUVA CUSTOMER? NO , IS THERE A TREND OBSERVED? NO , SUPPLIER ACTION AWARE

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24334275 ↗
  • MalfunctionFeb 13, 2026Contamination

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24334274 ↗
  • MalfunctionFeb 10, 2026Device Contamination with Chemical or Other Material

    DEFECT DESCRIPTION WAS INITIATED FOR AQL FAILURE FOR PARTICULATES. THE FTIR RESULTS CAME BACK WITH A 78 PERCENT CORRELATION TO SILICONE LUBRICANT. NO PATIENT HARM

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24305091 ↗
  • MalfunctionFeb 9, 2026Leak/Splash

    IT WAS REPORTED BY CUSTOMER THAT BATCHING SYRINGES LEAKING DRUG AT THE PLUNGER AREA OF THE SYRINGE. RCC RECEIVED A COMPLAINT VIA EMAIL. DATE: (B)(6) 2026 COMPLAINT NUMBER: (B)(4) ACCOUNT NUMBER: (B)(4) ITEM NUMBER: 308-305617 ,LOT# 5129980, EXPIRY 2030-04-30 LOT# 5195506 , EXPIRY 2030-06-30 SAMPLE AVAILABLE: YES ITEM DESCRIPTION: 20ML LUER-LOK TIP STERILE SYRINGE PACK INCIDENT DESCRIPTION: AS PER ACCOUNT, BATCHING SYRINGES LEAKING DRUG AT THE PLUNGER AREA OF THE SYRINGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24297522 ↗
  • MalfunctionFeb 9, 2026Leak/Splash

    IT WAS REPORTED BY CUSTOMER THAT BATCHING SYRINGES LEAKING DRUG AT THE PLUNGER AREA OF THE SYRINGE. RCC RECEIVED A COMPLAINT VIA EMAIL. DATE: 22.01.2026 COMPLAINT NUMBER: (B)(4), ACCOUNT NUMBER: (B)(4), ITEM NUMBER: 308-305617, LOT # / SERIAL #: LOT# 5129980, EXPIRY 2030-04-30 LOT# 5195506 , EXPIRY 2030-06-30 SAMPLE AVAILABLE: YES ITEM DESCRIPTION: 20ML LUER-LOK TIP STERILE SYRINGE PACK INCIDENT DESCRIPTION: AS PER ACCOUNT, BATCHING SYRINGES LEAKING DRUG AT THE PLUNGER AREA OF THE SYRINGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24297521 ↗
  • MalfunctionJan 30, 2026Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24222455 ↗
  • MalfunctionJan 30, 2026Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24222453 ↗
  • MalfunctionDec 13, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23798686 ↗
  • MalfunctionDec 10, 2025Leak/Splash; Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23770028 ↗
  • MalfunctionDec 10, 2025Leak/Splash; Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23770027 ↗
  • MalfunctionNov 10, 2025Leak/Splash; Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23518629 ↗
  • MalfunctionOct 24, 2025Leak/Splash; Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23378644 ↗
  • MalfunctionJun 15, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

    NO ADDITIONAL INFORMATION

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22208681 ↗
  • MalfunctionJun 3, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

    IT WAS REPORTED THAT BD SYRINGE 20ML LL TIP CONV PAK HAD FOREIGN MATTER. IT WAS REPORTED BY THE CUSTOMER THAT BLACK PARTICLE SEEN ON SOME SYRINGES. VERBATIM: BLACK PARTICLE SEEN ON SOME SYRINGES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22133476 ↗
  • MalfunctionMar 25, 2025Leak/Splash; Leak/Splash

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21688483 ↗
  • MalfunctionFeb 26, 2025Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT BD SYRINGE 20ML LL TIP CONV PAK LEAKED. IT WAS REPORTED BY CUSTOMER THAT LIQUID APPEARED TO HAVE LEAKED BEHIND SYRINGE PLUNGER ON A NUMBER OF SYRINGES IN THIS LOT. 11 SYRINGES CONTAINING CEFAZOLIN 2 G/20 ML HAVE BEEN SEQUESTERED. VERBATIM: RCC RECEIVED A COMPLAINT VIA COMMUNITY. PIR ATTACHED. LIQUID APPEARED TO HAVE LEAKED BEHIND SYRINGE PLUNGER ON A NUMBER OF SYRINGES IN THIS LOT. 11. SYRINGES CONTAINING CEFAZOLIN 2 G/20 ML HAVE BEEN SEQUESTERED. PRODUCT CODE: 305617.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21472313 ↗
  • MalfunctionFeb 3, 2025Break; Device Markings/Labelling Problem; Break; Device Markings/Labelling Problem

    NO ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21293874 ↗
  • MalfunctionJan 13, 2025Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT BD SYRINGE 20ML LL TIP CONV PAK LEAKED. IT WAS REPORTED BY THE CUSTOMER THAT FOUND TWO ADDITIONAL 20 ML LEAKING SYRINGES FROM THE SAME LOT (REF (B)(4), LOT: 4278835). VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. I FOUND TWO ADDITIONAL 20 ML LEAKING SYRINGES FROM THE SAME LOT (REF (B)(4) LOT: 4278835), SO I ALSO INCLUDED THESE SYRINGES IN THE TOTAL I AM SHIPPING TO YOU. I AM NOW SENDING TOTAL OF 19 SYRINGES FOR COMPLAINT (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21143082 ↗
  • MalfunctionDec 31, 2024Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT BD SYRINGE 20ML LL TIP CONV PAK LEAKED BATCH#: 4278835 AND AN UNKNOWN BATCH. IT WAS REPORTED BY THE CUSTOMER THAT LEAKING AT THE BACK OF THE PLUNGER. VERBATIM: (B)(6). RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. LEAKING AT THE BACK OF THE PLUNGER. 309605 LOT 4222762 TOTAL OF 18, 305617 LOT 4278835 TOTAL 17, 309680 LOT 1242178 TOTAL 4, XXXX. HAS SAMPLES AVAILABLE FOR INVESTIGATION PLEASE SEND PACKAGE THE SYRINGES HAS MEDICATION IN THEM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21048455 ↗
  • MalfunctionDec 13, 2024Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT BD SYRINGE 20 ML LL TIP CONV PAK LEAKED. IT WAS REPORTED BY CUSTOMER THAT THANK YOU FOR THE LABEL. SINCE THE INITIAL REPORT WE HAVE AN ADDITIONAL LOT THAT ALSO HAS BEEN AFFECTED. LOT 3333318. LEAKAGE. VERBATIM: COMPLAINT RECEIVED VIA EMAIL(S) ATTACHED. THANK YOU FOR THE LABEL. SINCE THE INITIAL REPORT WE HAVE AN ADDITIONAL LOT THAT ALSO HAS BEEN AFFECTED. LOT 3333318. LEAKAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20926569 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K110771. One submission often covers many models, so check the product and lot details in each record.

  • Z-2614-2026 · Apr 28, 2026 · Open, Classified
    SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston
  • Z-2753-2017 · Sep 16, 2016 · Terminated
    BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
  • Z-2747-2017 · Sep 16, 2016 · Terminated
    BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #305062
  • Z-2751-2017 · Sep 16, 2016 · Terminated
    BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
  • Z-2752-2017 · Sep 16, 2016 · Terminated
    BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injec
  • Z-2750-2017 · Sep 16, 2016 · Terminated
    BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #309580 The BD Single Use, Hypodermic Syringe is intended for use by health care prof
  • Z-2749-2017 · Sep 16, 2016 · Terminated
    BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G x 1 (0.6mm x 25mm) Catalog #309571 The BD Single Use, Hypodermic Syringe is intended for use by health care professi
  • Z-1936-2016 · Mar 25, 2016 · Terminated
    Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
  • Z-1937-2016 · Mar 25, 2016 · Terminated
    Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
  • Z-1055-2015 · Dec 19, 2014 · Terminated
    BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348, BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 4

Other Syringe, piston devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.