BD Safety-Lok 305902Recalls & reported problems

Summary

The FDA's MAUDE database contains 107 adverse event reports that list this exact device (DI 00382903059027), received between Nov 15, 2017 and Sep 10, 2026 — classified as 2 injuries, 105 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (22 reports).

4 other recalls cover devices cleared under the same FDA submission (K951254); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 107 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 10, 2026Material Twisted/Bent

  Two needles from the same lot number bent when trying to inject medication to a patient struggling against restraint. Needle bent on contact with patient skin, not when needle was in the patient's body. The first needle bent on "[redacted]" when trying to inject the patient and the second needle bent on "[redacted]"-the next day when trying to inject the same patient. The first needle bent at a 90- degree angle and the second needle bent in a curved fashion. Proper intramuscular injection technique was maintained (injecting at a 90-degree angle, securing and isolating the muscle, physical hold applied correctly). Both times required a second physical hold and delayed treatment of the patient as a second needle needed to be obtained for medication administration.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50713853 ↗
• MalfunctionApr 9, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 23X1 RB NEEDLE PULLED OUT OF HUB. COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. PER (B)(6) DURING A VACCINE INJECTION THE NEEDLE SEPARATED FROM THE HUB AND WAS LEFT IN THE PATIENT'S LEG. NO STRUGGLE/ISSUE WITH SHOT. IT JUST HAD SEPARATED AND LEFT NEEDLE IN THE LEG. HSI CONTROL NUMBER: 129056 HSI DESCRIPTION: SAFETYGLIDE NEEDLE HSI ITEM NUMBER: US_9875902 HSI MANUFACTURER PART NUMBER: 305902 HSI LOT OR SERIAL NUMBER: (B)(6).

  Patient problems: Insufficient Information

  MAUDE report 24831054 ↗
• MalfunctionMar 26, 2026Break

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 305902, BATCH # 5280958. VERBATIM: COMPLAINT VIA EMAIL. PLEASE REVIEW THE BRANDED PRODUCT QUALITY COMPLAINT INVOLVING HENRY SCHEIN ITEM# 9875902 FROM OUR CUSTOMER. THE CUSTOMER HAS BEEN ISSUED A RETURN LABEL TO RETURN THE PRODUCT FOR EVALUATION. PRODUCT DESCRIPTION: SAFETYGLIDE NEEDLE. HSI ITEM NUMBER: 9875902. MANUFACTURER PART NUMBER: 305902. LOT OR SERIAL NUMBER: LOT NUMBER: 5280958; EXPIRY DATE: 09/30/2030 ISSUE: ONE OF MY MEDICAL ASSISTANTS GAVE A VACCINE THIS MORNING, AND DURING THE INJECTION, THE NEEDLE ACTUALLY SEPARATED FROM THE HUB AND WAS ACTUALLY LEFT IN THE PATIENTS LEG? THERE WAS NO STRUGGLE OR ISSUE WITH THE SHOT, IT JUST WASLLEFT. PLEASE REACH OUT TO THE CUSTOMER DIRECTLY BY EMAIL AT OR BY PHONE AT IF YOU HAVE ANY ADDITIONAL QUESTIONS OR CONCERNS, AND TO PROVIDE THE FINDINGS OF YOUR INVESTIGATION. NO FURTHER DETAILS PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 24698225 ↗
• MalfunctionFeb 11, 2026Material Perforation

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 23X1 RB NEEDLE WENT THROUGH THE SHIELD. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. NEEDLE EMBEDDED INTO CAP AND PULLED OUT OF HUB WHEN CAP REMOVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24317472 ↗
• MalfunctionFeb 11, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 23X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. NEEDLE EMBEDDED INTO CAP AND PULLED OUT OF HUB WHEN CAP REMOVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24317063 ↗
• MalfunctionJan 15, 2026Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24089954 ↗
• MalfunctionOct 24, 2025Material Perforation; Material Perforation

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB NEEDLE WENT THROUGH THE SHIELD. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL #305902. LOT #5157464. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. PRODUCTCOMPLAINT - CUSTOMER CALLED TO REPORT THE BD 305902 LOT 5157464, HAD A BENT NEEDLE AND THIS WAS DISCOVERED WHILE OPENING THE PACKAGE, WHICH RESULTED IN A NEEDLE STICK OF A STAFF. SAMPLE IS AVAILABLE. DOE 10/06.

  Patient problems: Needle Stick/Puncture

  MAUDE report 23384000 ↗
• MalfunctionMar 27, 2025Activation Problem; Activation Problem

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB SAFETY MECHANISM DIFFICULT TO ACTIVATE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305902 BATCH#: 3352622. IT WAS REPORTED BY CUSTOMER THAT 2 DIFFERENT NURSES WERE STUCK BY NEEDLES WHEN TRYING TO COVER THE NEEDLE. THE NEEDLE BENT AND STUCK BOTH PEOPLE. RCC RECEIVED A COMPLAINT VIA EMAIL. ITEM(S): 305902 LOT(S): 3352622. DATE INCIDENT OCCURRED: LAST MONTH AND THEN TODAY (B)(6) 2025. WAS THE PATIENT IMPACTED? IF YES, DESCRIBE: 2 DIFFERENT NURSES WERE STUCK BY NEEDLES WHEN TRYING TO COVER THE NEEDLE. THE NEEDLE BENT AND STUCK BOTH PEOPLE. IS A SAMPLE AVAILABLE? NO. CUSTOMER REQUEST? PLEASE CALL. CONCERNED WITH FAULTY DESIGN. ADDITIONAL INFORMATION PROVIDED: AFTER FURTHER REVIEW, THE FIRST INCIDENT OCCURRED ON (B)(6) 2024. IT WAS NOT REPORTED. THE MA STATES AFTER SHE ADMINISTERED A VACCINE TO A PATIENT, SHE PUSHED DOWN THE SAFETY DEVICE USING TWO HANDS AND ACCIDENTLY PRICKED HER LEFT MIDDLE FINGER. SHE IS AN EXPERIENCED MA AND FEELS SOMETHING WAS WRONG WITH THE NEEDLE. IT IS A DIFFERENT LOT NUMBER BD SAFETY GLIDE 23GX1 REF 305902 LOT 33526. THE CORRECT LOT # IS 3352622.

  Patient problems: Needle Stick/Puncture

  MAUDE report 21709112 ↗
• MalfunctionMar 27, 2025Activation Problem; Activation Problem

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB SAFETY MECHANISM WAS DIFFICULT TO ACTIVATE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305902, BATCH#: 3352622. IT WAS REPORTED BY CUSTOMER THAT 2 DIFFERENT NURSES WERE STUCK BY NEEDLES WHEN TRYING TO COVER THE NEEDLE. THE NEEDLE BENT AND STUCK BOTH PEOPLE. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED ITEM(S): 305902 . LOT(S): 3352622. DATE INCIDENT OCCURRED:LAST MONTH AND THEN TODAY (B)(6) 2025. WAS THE PATIENT IMPACTED? IF YES, DESCRIBE: 2 DIFFERENT NURSES WERE STUCK BY NEEDLES WHEN TRYING TO COVER THE NEEDLE. THE NEEDLE BENT AND STUCK BOTH PEOPLE. IS A SAMPLE AVAILABLE?: NO. CUSTOMER REQUEST?: PLEASE CALL. CONCERNED WITH FAULTY DESIGN. ADDITIONAL INFORMATION PROVIDED: THE CORRECT LOT # IS 3352622.

  Patient problems: Needle Stick/Puncture

  MAUDE report 21708958 ↗
• MalfunctionMar 17, 2025Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21627497 ↗
• MalfunctionJan 14, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB NEEDLE WAS CLOGGED / BLOCKED. VERBATIM#: THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. 25X1 SAFETY GLADE. HAVING TROUBLE PUSHING THE DRUG THROUGH THE NEEDLE. JUST HAD TO RE-STICK THE PATIENT¿S 4TH DIFFERENT TIME OVER THE LAST MONTH (B)(6) LOT REJN0115. (B)(6) LOT 40954508. ADDITIONAL INFORMATION PROVIDED: 1. WHAT IS THE DATE OF EVENT FOR BOTH MATERIAL? THIS HAS HAPPENED A LOT OVER THE PAST SEVERAL MONTHS. 2. PLEASE SHARE THE CORRECT LOT NUMBER FOR MATERIAL 305916 LOT REJN0115 WE ALSO HAVE LOT 3333815 MATERIAL 305902 LOT 4095458 3. DESCRIBE ANY PATIENT HARM, INJURY, COMPLICATION OR NEGATIVE OUTCOME THAT OCCURRED AS A RESULT OF THE EVENT. NO PATIENT HARM OTHER THAN HAVING TO STICK THEM MULTIPLE TIMES. 4. ANY SAMPLE AVAILABLE FOR INVESTIGATION? IF YES, ARE YOU ABLE TO PROVIDE THE ADDRESS OF THE FACILITY FOR US TO SHIP THE RETURN LABEL? PLEASE MENTION THE MATERIAL FOR AVAILABLE SAMPLE. (B)(6). 5. PLEASE SHARE THE CAPTURED PHOTO OF THE EVENT IF AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21152558 ↗
• MalfunctionJan 3, 2025Device 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 21072712 ↗
• MalfunctionJan 2, 2025Activation Problem; Activation Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21055253 ↗
• MalfunctionDec 29, 2024Defective Component; Defective Component

  MATERIAL #: 305902, BATCH#: 4245513. IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB SAFETY MECHANISM IS DIFFICULT TO ACTIVATE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: COMPLAINT RECEIVED VIA EMAIL(S) ATTACHED. I GAVE A FLU SHOT THIS AFTERNOON AND THE NEEDLE SAFETY DID NOT FULLY COVER NEEDLE. NO INJURIES. ITEM -305902, LOT -4245513.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21032805 ↗
• MalfunctionDec 17, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20951621 ↗
• MalfunctionNov 21, 2024Complete Blockage; Complete Blockage

  MATERIAL # 305902 BATCH # 2318924, UNKNOWN IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB NEEDLE WAS CLOGGED / BLOCKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED ISSUE WITH 305902, LOT 2318924 ¿RN WAS TO ADMINISTER 80 MG OF IM METHYLPREDNISOLONE WITH A 3 ML SYRINGE AND A 23 G 1 INCH NEEDLE. HALF OF THE MEDICATION WAS ADMINISTERED THEN I MET RESISTANCE. I RETRACTED THE SYRINGE WITH THE NEEDLE STILL ATTACHED THE MEDICATION WOULD NOT ADVANCE, WHEN I REMOVED THE NEEDLE, THE MEDICATION WOULD ADVANCE THROUGH THE SYRINGE. I HAD TO ADMINISTER TWO SEPARATE INJECTIONS. THIS ALSO HAPPENED ON ANOTHER PATIENT WITH THE SAME MEDICATION AND SYRINGE/NEEDLE TYPE.¿ ADDITIONAL INFORMATION PROVIDED: 1. ONLY IMPACT TO THE PATIENT WAS THAT THEY RECEIVED TWO INJECTIONS 2. NO ADVERSE EFFECTS FROM THE INCIDENT 3. THE DATE IT OCCURRED WAS THE DATE THE MIDAS EVENT WAS PLACED. I AM UNABLE TO RECALL THE FIRST PATIENT AND WE SEE ANYWHERE THAT FROM 90-100 PATIENTS A DAY SO IT IS HARD FOR ME TO RECALL THE PATIENT INFORMATION 4. NO SAMPLE OR PHOTO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20754020 ↗
• MalfunctionOct 17, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  MATERIAL# 305902; BATCH# 4095458. IT WAS REPORTED THAT THE BD SAFETY-LOK NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. MA GAVE A VACCINE AND UPON PULLING THE NEEDLE OUT OF THE THIGH IT BECAME DETACHED FROM THE HUB.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20477206 ↗
• MalfunctionOct 14, 2024Leak/Splash; Leak/Splash

  MATERIAL #:309657; BATCH#:4116045. IT WAS REPORTED THAT THE BD SYRINGE 3ML LL 200 S/C LEAKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHILE ADMINISTERING DEPO INJECTION, MEDICATION BEGAN TO LEAK FROM HUB WHERE NEEDLE WAS INSERTED INTO SYRINGE, EVEN THOUGH IT WAS SCREWED IN TIGHTLY AND CORRECTLY. 305902 ALSO ATTACHED LOT # 4095458.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20444596 ↗
• MalfunctionOct 12, 2024Break; Break

  MATERIAL #: 305902. BATCH#: 4087139. IT WAS REPORTED THAT THE NEEDLE SFTYGLD 23X1 RB SAFETY MECHANISM BROKE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: COMPLAINT RECEIVED VIA EMAIL(S) ATTACHED. RCC RECEIVED A COMPLAINT VIA PHONE. (B)(6). REF: 305902. LOT: 4087139. REPORTER SAID MULTIPLE CLINICS HAVE REPORTED ISSUES ISSUE: 2 NEEDLE STICKS OCCURRED WITH 2 DIFFERENT MAS WHEN MEDICAL ASST. WERE ADMINISTERING VACCINES TO PEDIATRIC PTS. PRODUCT HAS A SAFETY DEVICE THAT YOU ACTIVATE WITH YOUR FINGER AND IT MALFUNCTIONED. IN ADDITION CUSTOMER IS REPORTING THAT THE NEEDLE IS THINNER AND WEAK CLINICIANS ARE NOT CONFIDENT IN THE RETRACTION FUNCTION. PT HARM: YES DIAGNOSTIC TESTING DID OCCUR AS A RESULT OF THE NEEDLE STICKS. REPRESENTATIVE SAMPLES OF THE REPORTED LOT ARE AVAILABLE FOR EVALUATION. SAMPLE RETURN KIT REQUESTED.

  Patient problems: Needle Stick/Puncture

  MAUDE report 20435240 ↗
• MalfunctionOct 12, 2024Break; Break

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Needle Stick/Puncture

  MAUDE report 20435239 ↗
• MalfunctionOct 10, 2024Leak/Splash; Leak/Splash

  MATERIAL #:305902; BATCH#:4095458. IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 23X1 RB LEAKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: WHILE ADMINISTERING DEPO INJECTION, MEDICATION BEGAN TO LEAK FROM HUB WHERE NEEDLE WAS INSERTED INTO SYRINGE, EVEN THOUGH IT WAS SCREWED IN TIGHTLY AND CORRECTLY. 305902 ALSO ATTACHED LOT # 4095458. ADDITIONAL INFORMATION PROVIDED: 1. PLEASE CONFIRM THE AFFECTED BATCH# OR LOT# NUMBER IS 4095458? ALSO ANOTHER LOT WAS MENTIONED IN BD PIR. PLEASE CONFIRM ANY ISSUE WITH THIS LOT# NUMBER 4116045? IF ANY ISSUE WITH THIS LOT# NUMBER 4116045, WHAT WAS THE ISSUE WITH THIS. GIVEN THIS OCCURRED BETWEEN THE SYRINGE AND THE NEEDLE, THE REPORTER GAVE BOTH LOT NUMBERS. THE OTHER LOT NUMBER IS APPARENTLY FROM THE 3 ML SYRINGE- ALSO A BD PRODUCT 2. IF SAMPLE AVAILABLE, KINDLY PROVIDE THE ADDRESS OF THE FACILITY FOR US TO SHIP THE RETURN LABEL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20424267 ↗
• MalfunctionSep 24, 2024Complete Blockage; Complete Blockage

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20297086 ↗
• MalfunctionSep 24, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THIS IS NOT A BD DEVICE PER CUSTOMER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20295702 ↗
• MalfunctionAug 21, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  MATERIAL#: 305902. BATCH#: 4082651. IT WAS REPORTED THAT THE BD SAFETY-LOK NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. INJURIES OR ADVERSE EVENT: NO ITEM: 305902 QUANTITY AFFECTED: 1 BX. SERIAL/LOT NUMBER: (B)(4). PO : (B)(4). ARE ANY SAMPLES AVAILABLE FOR RETURN? YES REPORTED ISSUE: 7/31 CST EMAILED IN STATING THAT THE NEEDLE CAME OUT OF THE HUB AND STAYED IN THE PATIENT THIGH, SAFETY SLIDE MALFUNCTION ADDITIONAL INFORMATION PROVIDED: THERE WASN¿T ANY SERIOUS INJURY TO THE PATIENT OR TO MYSELF. THE DATE OF THE INCIDENT WAS AROUND (B)(6) 2024.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20022777 ↗
• MalfunctionJun 17, 2024Separation Problem; Separation Problem

  MATERIAL: 305902. BATCH#: 3312251. IT WAS REPORTED BY THE CUSTOMER THAT ADMINISTERING FLU VACCINE TO PATIENT. AFTER PUSHING PLUNGER DOWN AND PULLED BACK, THE NEEDLE WAS DISCONNECTED FROM PLUNGER AND IN PATIENT¿S LEG. MEDICAL ASSISTANT (MA) PULLED NEEDLE OUT OF LEG USING A GLOVED HAND. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. ADMINISTERING FLU VACCINE TO PATIENT. AFTER PUSHING PLUNGER DOWN AND PULLED BACK, THE NEEDLE WAS DISCONNECTED FROM PLUNGER AND IN PATIENT¿S LEG. MEDICAL ASSISTANT (MA) PULLED NEEDLE OUT OF LEG USING A GLOVED HAND. MODEL# 305902; LOT# 3312251. CUSTOMER RESPONSE: CAN YOU SHARE ANY PHYSICAL SAMPLE OR PHOTO IF AVAILABLE FOR INVESTIGATION? NOT AVAILABLE: DISCARDED. ANY ADVERSE EVENT OR SERIOUS INJURY REPORTED TO PATIENT OR HEALTHCARE PROFESSIONAL? IF YES, PLEASE PROVIDE THE DETAILS. NONE. COULD YOU PLEASE CONFIRM IS THERE ANY LEAK. UNKNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19554780 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K951254. One submission often covers many models, so check the product and lot details in each record.

• Z-2889-2020 · Jul 28, 2020 · Terminated
  BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
• Z-0315-2018 · Jul 5, 2017 · Terminated
  SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.
• Z-3116-2017 · Jun 13, 2017 · Terminated
  BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from
• Z-2748-2017 · Sep 16, 2016 · Terminated
  BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below th