BD Luer-Lok 309575Recalls & reported problems

Summary

The FDA's MAUDE database contains 54 adverse event reports that list this exact device (DI 30382903095750), received between Dec 21, 2017 and Sep 15, 2026 — classified as 54 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (14 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.

Most reported problems

Recent adverse event reports

The 25 most recent of 54 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 15, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50778991 ↗
• MalfunctionSep 15, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50778978 ↗
• MalfunctionApr 3, 2026Leak/Splash

  IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL 21X1 RB HAD LEAKAGE PAST THE STOPPER. VERBATIM: COMPLAINT VIA EMAIL. EARLIER TODAY, ONE OF MY DISPENSERS NOTICED THAT THEIR SYRINGE WAS LEAKING DOWN THE PLUNGER AND HAD LEAKED THROUGH THE RUBBER STOPPER PIECE. I HAVE ATTACHED THE IMAGES. IT IS LITTLE DIFFICULT TO TELL AS THE DISPENSERS MUST USE A SYRINGE SHIELD, BUT THE LIQUID IS FAINTLY VISIBLE WITHIN THE SHIELD. CAN YOU PLEASE PROVIDE AN EXACT DATE OF EVENT IN FORMAT DD-MMM-YYYY: 10-MAR-2026. CAN YOU PLEASE PROVIDE THE MATERIAL AND LOT NUMBER ASSOCIATED WITH REPORTED ISSUE: MATERIAL NUMBER - 309575, LOT # - 5241754. ANY SAMPLE AVAILABLE FOR INVESTIGATION? IF YES, ARE YOU ABLE TO PROVIDE THE ADDRESS OF THE FACILITY FOR US TO SHIP THE RETURN LABEL: NO, THE DEFECT WAS FOUND ON THE SYRINGE WHILE FILLING A DOSE. - THE SYRINGE IS CONTAMINATED. DESCRIBE ANY PATIENT HARM, INJURY, COMPLICATION OR NEGATIVE OUTCOME THAT OCCURRED AS A RESULT OF THE EVENT: SLOWED DOWN PRODUCTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24776490 ↗
• MalfunctionJan 13, 2026Connection Problem

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24063089 ↗
• MalfunctionJan 13, 2026Connection Problem

  IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL 21X1 RB DEMONSTRATED CONNECTION ISSUES. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL: I AM WRITING TO BRING TO YOUR ATTENTION AN ISSUE WITH THE 3 ML SYRINGES WE RECEIVED FOR THE LOT NUMBER MENTIONED IN THE ATTACHED FORM. WE HAVE IDENTIFIED NUMBER OF DEFECTIVE 3 ML SYRINGES WITHIN THE CASES RECEIVED. SPECIFICALLY, THE SYRINGE PLUNGER SEAL IS NOT PROPERLY INTACT ON SEVERAL UNITS FOUND IN THE BOXES. ADDITIONALLY, SOME OF THE SYRINGES WE FOUND WITH LOOSE NEEDLES IN THE PACK. FOR YOUR REFERENCE AND FURTHER REVIEW, I HAVE ATTACHED PHOTOS SHOWING EXAMPLES OF THE DEFECTIVE SYRINGES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24063085 ↗
• MalfunctionJan 6, 2026Contamination /Decontamination Problem

  IT WAS REPORTED THAT BD SYRINGE 3ML LL W/NDL 21X1 RB CONTAINED FOREIGN MATTER. 1.SPECIFY THE PENDING AFFECTED QUANTITIES IN CASES/EACH/UNIT FOR THE CREDIT PROCESS. INITIALLY 5 CASES, THEN A FURTHER 8 CASES IDENTIFIED (DISCUSSED AS 13 CS), LASTLY A 4.5 CASES (36 BOXES) 2.PROVIDE THE LOT NUMBER(S). ALL LOT 4354918 3.CONFIRM WHETHER THE ISSUE IDENTIFICATION DATE IS THE SAME AS AUGUST 12 OR A DIFFERENT DATE. IF IT IS A DIFFERENT DATE, PLEASE PROVIDE THE RESPECTIVE DATE OF ISSUE IDENTIFICATION. WE WERE ADVISED SEPTEMBER 3RD, 8TH AND 11TH AS THE ADDITIONAL QUANTITIES WERE NOTED EARLIER THIS YEAR WE RECEIVED A LOT NUMBER OF 3CC SYRINGES (4354918) FROM BD THAT HAVE ONLY RECENTLY BEEN USED IN OUR PRODUCTION. UPON VISUAL INSPECTION OF THESE SYRINGES, IT HAS BEEN NOTED THAT THERE HAVE BEEN MANY SYRINGES WITH SOME SORT OF ADHESIVE/PARTICULATE ON THE NEEDLE ITSELF. FOR OBVIOUS REASONS, WE ARE UNABLE TO USE THESE SYRINGES AND ARE REJECTING APPROXIMATELY 5 CASES (4,000 SYRINGES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23978457 ↗
• MalfunctionJan 6, 2026Contamination /Decontamination Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23978455 ↗
• MalfunctionJan 6, 2026Contamination /Decontamination Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23978448 ↗
• MalfunctionDec 13, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL 21X1 RB HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 309575. BATCH # 5083505. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. WE WOULD LIKE TO REPORT AN ISSUE RELATED TO 3CC SYRINGE (309575) LOT # 5083505, EXPIRATION 28 FEB 2030 (02-28-2030). ON 12 NOV 2025 (11-12-2025), IT WAS REPORTED BY ONE OF OUR CUSTOMERS THAT A BROWN SUBSTANCE WAS OBSERVED ON THE BARREL OF THE SYRINGE NEAR THE FLANGE. THE SYRINGE WAS RETURNED TO US TODAY, AND UPON INVESTIGATION, THE BROWN SUBSTANCE SEEMS TO BE INCORPORATED IN THE PLASTIC (IT DID NOT SCRAPE OFF OR WIPE OFF WITH IPA). PLEASE SEE ATTACHED PHOTOS. I HAVE KEPT THE PHYSICAL SYRINGE, AS IT WAS NOT INJECTED INTO A PATIENT, IF REQUIRED TO SEND TO YOU FOR INVESTIGATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23798681 ↗
• MalfunctionAug 13, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL 21X1 RB HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER; MATERIAL #309575 LOT #4354918 VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. LAST MONTH WE RECEIVED PRODUCT CODE 309575, LOT NUMBER 435918 OF 3CC SYRINGES. AT THE BEGINNING OF THE MONTH OF JULY, WE STARTED USING THE LOT NUMBER IN PRODUCTION AND SOME OF OUR TECHNICIANS HAVE NOTICED THERE IS SOMETHING STUCK TO THE NEEDLES OF A SIGNIFICANT AMOUNT OF THE SYRINGES. THE TECHNICIANS HAVE BEEN ASKED TO REMOVE THESE SYRINGES FROM PRODUCTION WHEN THEY NOTICE SOMETHING STUCK TO THE NEEDLE AS WE CANNOT AFFORD TO HAVE PARTICULATE ON A NEEDLE AND INJECTED INTO A PATIENT. THIS ISSUE WAS NOTICED DURING THE FIRST WEEK OF (B)(6). ADDITIONAL INFORMATION PROVIDED; 1. IF POSSIBLE, COULD YOU PLEASE CONFIRM THE EXACT DATE OF THE EVENT IN THE FORMAT DD-MMM-YYYY? 24 JUL 2025 2. LOT NUMBER [435918] WAS NOT MATCH WITH MATERIAL NUMBER [ 309575 - SYRINGE 3ML LL W/NDL 21X1 RB]. COULD YOU PLEASE CHECK AND RECONFIRM THE LOT NUMBER? THE LOT NUMBER IS 4354918 3. COULD YOU PLEASE RECONFIRM WHETHER THE SAMPLE IS AVAILABLE FOR OUR INVESTIGATION? YES, THE SYRINGE

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22800379 ↗
• MalfunctionJul 18, 2025Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL 21X1 RB STOPPER WAS JAMMED / INSECURE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 309575, LOT#: 4354917. RCC RECEIVED A COMPLAINT VIA EMAIL. TODAY, WE FOUND TWO BD PLASTIPAK 3ML SYRINGE-LUER-LOK TIP WITH BD PRECISIONGLIDE NEEDLE. (LOT#: 4354917) THAT THE RUBBER TIP/STOPPER WAS NOT PROPERLY APPLIED TO THE PLUNGER. THIS CAUSED THE MEDICATION TO LEAK AROUND THE PLUNGER AND THE LUER-LOK NEEDLE. I WANTED TO BRING THIS TO YOUR ATTENTION IN CASE THERE HAVE ANY OTHER REPORTED DEFECTIVE SYRINGES. ADDITIONAL INFORMATION PROVIDED: 1. COULD YOU PLEASE RECONFIRM AN EXACT DATE OF EVENT IN THIS FORMAT MM-DD-YYYY? 7/8/2025. 2. CAN YOU SHARE ANY PHYSICAL SAMPLE IF AVAILABLE FOR INVESTIGATION? 3. DESCRIBE ANY PATIENT HARM, INJURY, COMPLICATION OR NEGATIVE OUTCOME THAT OCCURRED AS A RESULT OF THE EVENT. MEDICATION LEAKED AND UNABLE TO ADMINISTER TO PATIENT. MEDICATION HAD TO BE WASTED AND REPLACED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22548796 ↗
• MalfunctionJul 17, 2025Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22535049 ↗
• MalfunctionFeb 19, 2025Connection Problem; Connection Problem

  NO ADDITIONAL INFORMATION WAS PROVIDED

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21416073 ↗
• MalfunctionJan 24, 2025Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21233826 ↗
• MalfunctionNov 14, 2024Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20682861 ↗
• MalfunctionOct 20, 2024Defective Component; Defective Component

  MATERIAL # 309575; BATCH # 4221164. IT WAS REPORTED THAT THE BD LUER-LOK NEEDLE HUB HAD A HOLD /CRACK / WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. MY STAFF AT OUR CLEANROOM INFORMED ME THAT THEY WERE HAVING ISSUES WITH A FEW OF THE BD PLASTIPAK 3 ML SYRINGES. THEY SAID THAT LOOKS LIKE THERE¿S A HOLE IN THE HUB AND THAT WHEN THEY WERE RETRIEVING DRUG THE DRUG WAS COMING OUT FROM THE HOLE IN THE HUB. LOT # 4221164. I DON¿T THINK IT WILL BE POSSIBLE TO SEE IN THE PICTURE, BUT I DO HAVE AT LEAST ONE SYRINGE WITH ME IF YOU WANT IT TO BE INSPECTED. ADDITIONAL INFORMATION PROVIDED: THE EXACT DATE OF EVENTS WAS ON 09/27/2024. MY TECH ONLY INFORMED ME OF TWO TIMES THAT THIS HAPPENED TO HER. THE EVENTS HAPPENED WITH TWO MEDICATIONS: ONDANSETRON AND MICAFUNGING. NO IMPACT ON PATIENT. IT ONLY DELAYED A LITTLE TIME IN THE PROCESS OF COMPOUNDING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20490227 ↗
• MalfunctionSep 17, 2024Defective Component; Defective Component

  MATERIAL#: 309575 BATCH NUMBER#: 2188396 IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL 21X1 RB NEEDLE HUB HAD A HOLE / WAS CRACKED / DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM#: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. REF: 309575 LOT: 2188396 ISSUE: CUSTOMER IS REPORTING THAT THE ASSEMBLED SYRINGE NEEDLE COMBOS NEEDLE HUB WAS BENT NOT THE NEEDLE, THE NEEDLE WAS STRAIGHT. NO SAMPLE OF THIS IS AVAILABLE FOR INVESTIGATION. NO PT HARM DOE 28AUG2024 AND UNKNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20242272 ↗
• MalfunctionSep 17, 2024Defective Component; Defective Component

  MATERIAL#: 309575. BATCH NUMBER#: 2188396. IT WAS REPORTED THAT THE BD SYRINGE 3ML LL W/NDL 21X1 RB NEEDLE HUB HAD A HOLE / WAS CRACKED / DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM#: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. REF: (B)(4). LOT: 2188396. ISSUE: CUSTOMER IS REPORTING THAT THE ASSEMBLED SYRINGE NEEDLE COMBOS NEEDLE HUB WAS BENT NOT THE NEEDLE, THE NEEDLE WAS STRAIGHT. NO SAMPLE OF THIS IS AVAILABLE FOR INVESTIGATION. NO PT HARM. DOE (B)(6) 2024 AND UNKNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20242270 ↗
• MalfunctionJul 10, 2024Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19715347 ↗
• MalfunctionJun 9, 2024Volume Accuracy Problem; Volume Accuracy Problem

  MATERIAL#:309575, BATCH#: 3331068. IT WAS REPORTED BY THE CUSTOMER THAT THE A FACILITY ADMINISTRATOR REPORTED TO XXXX THAT A BD 3ML LUER-LOK SYRINGE 21GX1IN HAD NO MILLILITER MARKINGS. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COMPLAINT#: (B)(4). PRODUCT: BD 3ML LUER-LOK SYRINGE 21GX1IN. PRODUCT #: 309575. LOT#: 3331068. COMPLAINT: A FACILITY ADMINISTRATOR REPORTED TO XXXXX THAT A BD 3ML LUER-LOK SYRINGE 21GX1IN HAD NO MILLILITER MARKINGS. DEAR QA DEPARTMENT: THE PURPOSE OF THIS LETTER IS TO NOTIFY YOU, THE MANUFACTURER THAT XXXX. NA, DISTRIBUTOR OF YOUR BD 3ML LUER-LOK SYRINGE 21GX1IN, RECEIVED THE ABOVE COMPLAINT AGAINST THIS PRODUCT. COMMENTS ON 05/06/2024. ALL AVAILABLE INFORMATION HAS BEEN PROVIDED, REGULATORY REPORTING IS THE RESPONSIBILITY OF THE MANUFACTURER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19495350 ↗
• MalfunctionDec 5, 2023Crack; Crack

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18269803 ↗
• MalfunctionDec 5, 2023Crack; Crack

  MATERIAL#: UNKNOWN. BATCH#: UNKNOWN. IT WAS REPORTED BY THE CUSTOMER THAT HERE IS THE INFO FOR THE 3ML SYRINGES REPORTED WITH CRACKS. 3 ML BD LUER-LOK¿ SYRINGE WITH ATTACHED NEEDLE 21 G X 1 IN., STERILE, SINGLE USE. OUR IR DEPT REPORTED TO US THAT ITEM 56572 SYRINGES HAVE CRACKS/HOLES IN THE SIDE OF THE SYRINGE AND WHEN PRESSING THE SYRINGE THE MEDICATION IS LEAKING OUT OF THE SIDE. I WITNESSED THIS HAPPENING. THEY FOUND 4 JUST THIS MORNING LEAKING. RIGHT NOW IT¿S ONLY BEEN DETECTED IN ONE LOT. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. HERE IS THE INFO FOR THE 3ML SYRINGES REPORTED WITH CRACKS. 3 ML BD LUER-LOK¿ SYRINGE WITH ATTACHED NEEDLE 21 G X 1 IN., STERILE, SINGLE USE. OUR IR DEPT REPORTED TO US THAT ITEM 56572 SYRINGES HAVE CRACKS/HOLES IN THE SIDE OF THE SYRINGE AND WHEN PRESSING THE SYRINGE THE MEDICATION IS LEAKING OUT OF THE SIDE. I WITNESSED THIS HAPPENING. THEY FOUND 4 JUST THIS MORNING LEAKING. RIGHT NOW IT¿S ONLY BEEN DETECTED IN ONE LOT. COMMENTS ON 17-NOV-2023. 1. PLEASE PROVIDE THE MATERIAL NUMBER AND BATCH NUMBER. MATERIAL # 309575 BATCH # 3135920 ALSO, FOUND A CRACK IN 309575 BATCH # 3135922. 2. IS THERE ANY SAMPLE AVAILABLE FOR INVESTIGAT

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18269786 ↗
• MalfunctionOct 30, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18035906 ↗
• MalfunctionJul 11, 2023Crack; Crack

  IT WAS REPORTED THAT DURING USE WITH BD PLASTIPAK¿ LUER-LOK¿ TIP SYRINGE WITH BD PRECISIONGLIDE¿ NEEDLE THE BARREL WAS DISCOVERED TO BE CRACKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CUSTOMER OBSERVED A CRACKED SYRINGE BARREL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17301436 ↗
• MalfunctionJun 30, 2023Defective Component; Defective Component

  IT WAS REPORTED WHILE USING BD SYRINGE 3ML LL W/NDL 21X1 RB THE PLUNGER WAS DIFFICULT TO MOVE. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: DETAILS OF COMPLAINT (REPORTED ISSUE): WE HAVE RECEIVED OUR SHIPMENT, BUT DURING INSPECTION ONE OF THE BATCHES OF 3CC SYRINGES FAILED INSPECTION. COMPLAINT CATEGORY: FAIL TO FUNCTION / DEFECTIVE. INCIDENT DATE: (B)(6) 2023. COMPLAINT NOTICED: PRIOR TO USE. PROBLEM FREQUENCY: 1ST TIME. CUSTOMER EXPOSURE: PATIENT INJURY: NO. QTY AFFECTED: 3 CA. SAMPLES AVAILABLE? YES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17239273 ↗

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-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-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-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-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-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-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