BD SafetyGlide 305916Recalls & reported problems

Summary

The FDA's MAUDE database contains 1,767 adverse event reports that list this exact device (DI 00382903059164), received between Oct 17, 2017 and Sep 1, 2026 — classified as 13 injuries, 1,754 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (1,236 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 16, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 1,767 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 1, 2026Contamination

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50547345 ↗
• MalfunctionJun 11, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: COMPLAINT VIA EMAIL. WE ORDER OUR BD SAFETY GLIDES THROUGH X. BUT I WANTED REPORT DEFECTIVE NEEDLES TO THE COMPANY JUST INCASE THERE WAS A RECALL L 25GX1INCH NEEDLES LOT 2010821 EXPIRATION 12/31/2026 THE NEEDLE ARE EITHER CLOSED OR TOO SMALL TO PUSH VACCINE THROUGH LOT 4327957 EXPIRATION 10/31/2029 THE NEEDLE DISCONNECTED FROM THE CONNECTION AND STAYED IN THE PATIENT. THE PATIENT WAS NOT HARMED, AND THE NEEDLE WAS REMOVED FROM THE PATIENTS ARM, BUT THIS COULD HAVE BEEN TERRIBLE IF THIS WAS A CHILD. THE NURSES USING THE NEEDLES HAVE MANY YEARS OF EXPERIENCE THIS WAS NOT USER ERROR. BOTH NURSES HAVE BEEN GIVING FOR 10 PLUS YEARS. PLEASE LET ME KNOW WHAT OTHER INFORMATION YOU NEED TO IDENTIFY THESE DEFECTIVE NEEDLES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25472384 ↗
• MalfunctionApr 30, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED REPORT INCIDENT OR PROBLEM INFORMATION. REFERENCE NUMBER (ID): (B)(4). DATE OF INCIDENT (YYYY-MM-DD): (B)(6) 2026. SITE NAME/LOCATION: LEVEL OF HARM: TEMPORARY HARM. ALBERTA OPTIONAL REPORT TO CMDSNET (HEALTH CANADA): YES. INCIDENT DETAILS: PATIENT REQUIRED HALDOL INTRAMUSCULAR INJECTION, UPON ADMINISTRATION TO L THIGH AND REMOVAL OF NEEDLE- NEEDLE REMAINED IN THIGH AND SEPARATED FROM PLASTIC PIECE. PATIENT THRASHING AROUND, ADVISED PATIENT TO RELAX, WRITER WAS ABLE TO REMOVE NEEDLE MANUALLY. WHO WAS AFFECTED? PATIENT PROCEDURE: BD SAFETY GLIDE NEEDLE 25 G X 1 - INTRAMUSCULAR INJECTION DEVICE INFORMATION DEVICE NAME/DESCRIPTION: NEEDLE HYPODERMIC SAFETY 25GA X 1 IN MANUFACTURER: MANUFACTURER CODE/MODEL: 305916. SERIAL OR LOT NUMBER: (B)(6) DEVICE EXPIRY DATE (YYYY-MM-DD): 2027-09-30. SUPPLIER: SUPPLIER CATALOGUE NUMBER: (B)(4). WAS THE DEVICE RETAINED? NO. INVESTIGATION REQUEST. EXPECTED TYPE OF INVESTIGATION: LOT REVIEW. CLINICAL CONTACT INFORMATION. MANAGER (CC ON FINAL REPORT): FILING REFERENCE ID: (B)(4). END OF REPORT. YES, THE METAL NEEDLE SEPARATED FROM T

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25046956 ↗
• MalfunctionApr 14, 2026Leak/Splash; Connection Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24877037 ↗
• MalfunctionApr 2, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 21X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: THREE INCIDENTS OF SAFETYGLIDE NEEDLES DETACHING FROM THE HUB, RESULTING IN THE NEEDLE BEING LEFT IN THE PATIENT. THE NEEDLES HAD TO BE MANUALLY REMOVED FROM THE PATIENTS. ALL OF THESE WERE ITEM 305916. ADDITIONAL INFORMATION RECEIVED ON 19-MAR-2026: TEAM- I CAN PROVIDE THIS INFORMATION, SINCE PRISMA ALREADY SHARED THIS WITH ME: 1. (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT # 5197895 EX 6/30/2030. ORDERED THROUGH. 2. (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT # 5174468 EX 5/31/30. ORDERED THROUGH. 3. (B)(6) 2026: ADMINISTRATION OF VACCINE, ONCE NEEDLE PLACED IN THIGH THE NEEDLE BENT AND VACCINE COULD NOT BE ADVANCED FROM THE SYRINGE BD 1 IN SAFETY GLIDE NEEDLE 25G LOT # 5246356 EXPIRATION 8-31-30. ORDERED THROUGH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24769031 ↗
• MalfunctionApr 2, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 21X1 RB NEEDLE PULLED OUT OF HUB. THREE INCIDENTS OF SAFETYGLIDE NEEDLES DETACHING FROM THE HUB, RESULTING IN THE NEEDLE BEING LEFT IN THE PATIENT. THE NEEDLES HAD TO BE MANUALLY REMOVED FROM THE PATIENTS. ALL OF THESE WERE ITEM 305916. ADDITIONAL INFORMATION RECEIVED ON 19-MAR-2026: TEAM- I CAN PROVIDE THIS INFORMATION, SINCE PRISMA ALREADY SHARED THIS WITH ME: 1. (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT # 5197895 EX 6/30/2030. ORDERED THROUGH. 2. (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT # 5174468 EX 5/31/30. ORDERED THROUGH. 3. (B)(6) 2026: ADMINISTRATION OF VACCINE, ONCE NEEDLE PLACED IN THIGH THE NEEDLE BENT AND VACCINE COULD NOT BE ADVANCED FROM THE SYRINGE BD 1 IN SAFETY GLIDE NEEDLE 25G LOT # 5246356 EXPIRATION 8-31-30. ORDERED THROUGH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24767655 ↗
• MalfunctionApr 2, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 21X1 RB NEEDLE PULLED OUT OF HUB. THREE INCIDENTS OF SAFETYGLIDE NEEDLES DETACHING FROM THE HUB, RESULTING IN THE NEEDLE BEING LEFT IN THE PATIENT. THE NEEDLES HAD TO BE MANUALLY REMOVED FROM THE PATIENTS. ALL OF THESE WERE ITEM: 305916. ADDITIONAL INFORMATION RECEIVED ON 19-MAR-2026: TEAM. I CAN PROVIDE THIS INFORMATION, SINCE PRISMA ALREADY SHARED THIS WITH ME: 1. ON (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT#: 5197895, EX: 6/30/2030. ORDERED THROUGH. 2. ON (B)(6) 2026: ADMINISTERED VACCINE, ONCE THE NEEDLE PLACED IN THE THIGH, NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. HAD TO BE MANUALLY REMOVED FROM THIGH. BD SAFETY GLIDE NEEDLE 25G X 1 LOT#: 5174468, EX 5/31/2030. ORDERED THROUGH. 3. ON (B)(6) 2026: ADMINISTRATION OF VACCINE, ONCE NEEDLE PLACED IN THIGH THE NEEDLE BENT AND VACCINE COULD NOT BE ADVANCED FROM THE SYRINGE BD 1 IN SAFETY GLIDE NEEDLE 25G LOT#: 5246356 EXPIRATION 8-31-2030. ORDERED THROUGH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24767651 ↗
• MalfunctionMar 19, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. DURING ADMINISTRATION OF VACCINES, ON TWO SEPARATE OCCASIONS, THE 25G 1" NEEDLE BECAME LOOSE FROM THE HUB AND REMAINED IN THE PEDIATRIC PATIENT'S SKIN FOLLOWING THE INJECTION. THE NEEDLE WAS REMOVED BY THE TEAM MEMBER. NO PATIENT HARM NOTED FOR EITHER PATIENT. THIS REPORT INVOLVES TWO SEPARATE PEDIATRIC PATIENTS WITH 2 DIFFERENT LOT NUMBERS OF THE SAME GAUGE AND LENGTH BD SAFETYGLIDE NEEDLE. LOT NUMBERS INVOLVED PATIENT #1 (B)(6) 2026 LOT 5197895 EXP 6/30/2030. PATIENT #2 (B)(6) 2026 LOT 5174468 EXP 5/31/2030. HEALTH EFFECT CODE: 4582. DEVICE PROBLEM CODE: 1371, 3015.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24640656 ↗
• MalfunctionMar 19, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB NEEDLE PULLED OUT OF HUB. RCC RECEIVED A COMPLAINT VIA EMAIL. DURING ADMINISTRATION OF VACCINES, ON TWO SEPARATE OCCASIONS, THE 25G 1" NEEDLE BECAME LOOSE FROM THE HUB AND REMAINED IN THE PEDIATRIC PATIENT'S SKIN FOLLOWING THE INJECTION. THE NEEDLE WAS REMOVED BY THE TEAM MEMBER. NO PATIENT HARM NOTED FOR EITHER PATIENT. THIS REPORT INVOLVES TWO SEPARATES PEDIATRIC PATIENTS WITH 2 DIFFERENT LOT NUMBERS OF THE SAME GAUGE AND LENGTH BD SAFETYGLIDE NEEDLE. LOT NUMBERS INVOLVED PATIENT #1 (B)(6) 2026 LOT 5197895 EXP 6/30/2030. PATIENT #2 (B)(6) 2026 LOT 5174468 EXP 5/31/2030. HEALTH EFFECT CODE: 4582. DEVICE PROBLEM CODE: 1371, 3015.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24640654 ↗
• MalfunctionMar 12, 2026Contamination

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB CONTAINED FOREIGN MATTER. VERBATIM: POSSIBLE MOLD INSIDE INDIVIDUAL PRODUCT PACKAGING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24583559 ↗
• MalfunctionMar 10, 2026Break

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24559252 ↗
• MalfunctionFeb 27, 2026Break

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24470141 ↗
• MalfunctionFeb 9, 2026Detachment of Device or Device Component

  THERE WAS NO PATIENT HARM, INJURY, COMPLICATION OR NEGATIVE OUTCOME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24294021 ↗
• MalfunctionJan 30, 2026Material Perforation

  IT WAS REPORTED THAT DURING THE ATTEMPT AT PERIPHERAL VENOUS PUNCTURE, IT WAS OBSERVED THAT TWO INTRAVENOUS CATHETERS, BOTH WITH SAFETY DEVICES, HAD BENT TIPS AT THE MOMENT OF INSERTION, WITH OPENING/COLLAPSE OF THE CANNULA, WHICH RESULTED IN INJURY AND RUPTURE OF THE VEIN USED DURING THE PROCEDURE, MAKING IT IMPOSSIBLE TO CONTINUE THE PUNCTURE.

  Patient problems: Perforation of Vessels

  MAUDE report 24226010 ↗
• MalfunctionJan 29, 2026Break

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24210916 ↗
• MalfunctionJan 28, 2026Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB NEEDLE PULLED OUT OF HUB. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. INFANT RECEIVED 2-MONTH IMMUNIZATION. THIRD VACCINE PROVIDED WAS PNEUMOC15 TO RIGHT LEG. AFTER INJECTING VACCINE TO R LEG, SYRINGE WAS REMOVED. NEEDLE REMAINED TO R LEG, HORIZONTAL, ALMOST COMPLETELY VISIBLE. NEEDLE HAD DETACHED FROM HUB OF NEEDLE WRITER QUICKLY REMOVED NEEDLE FROM LEG AND PLACED NEEDLE IN SHARPS CONTAINER, WRITER PLACED SYRINGE IN SHARPS CONTAINER. WRITER REASSURED PARENTS THAT INFANT RECEIVED ENTIRE DOSE OF VACCINE, AND THAT ENTIRE NEEDLE WAS OUT OF LEG, NO PART OF NEEDLE LEFT IN LEG.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24203038 ↗
• MalfunctionJan 26, 2026Activation Problem

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB -SAFETY MECHANISM BROKE. RCC RECEIVED A COMPLAINT VIA EMAIL. INCIDENT OR PROBLEM INFORMATION INCIDENT DETAILS: AFTER ADMINISTERING VACCINE TO CLIENT, WRITER ATTEMPTED TO DEPLOY THE SAFETY MECHANISM ON THE NEEDLE. SAFETY CAME DETACHED FROM NEEDLE AND FLEW INTO ADJACENT WALL WHERE IT CAME TO REST ON THE FLOOR. WRITER DISPOSED OF USED NEEDLE AS IT WAS CONTAMINATED, WAS UNSURE OF WHETHER SAFETY MECHANISM TOUCHED NEEDLE SO ENCLOSED IN AN ALCOHOL WIPE AND WRAPPER AND BROUGHT BACK TO CHC WHERE IT WAS PLACED INTO A PLASTIC CONTAINER AND STORED IN DESK. IMPACT OF INCIDENT: WHO WAS AFFECTED? PATIENT UNEXPECTED OR PROLONGED CARE? YES FREQUENCY OF PROBLEM: FIRST TIME. DEVICE INFORMATION DEVICE NAME/DESCRIPTION: NEEDLE HYPODERMIC SAFETY 25GA X 1 IN. MANUFACTURER CODE/MODEL: 305916 SERIAL OR LOT NUMBER: NOT PROVIDED EXPIRY DATE: SUPPLIER/CATALOGUE NUMBER: 308-305916 IS THE DEVICE RETAINED? YES NUMBER OF DEVICES: 1 WIPED, CONTAINED, LABELLED? WIPED, DOUBLE BAGGED (IF CONSUMABLE), AND LABELLED AS PER INSTRUCTIONS. DEVICE HANDLING HAZARDS (WHEN BLANK = HAZARDS NOT SPECIFIED) BLOOD AND/OR BODY FLUID CONTAMINATED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24179831 ↗
• MalfunctionJan 16, 2026Activation Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: Needle Stick/Puncture

  MAUDE report 24093048 ↗
• MalfunctionJan 15, 2026Connection Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24088350 ↗
• MalfunctionJan 6, 2026Activation Problem

  IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 25X1 RB SAFETY MECHANISM WAS DIFFICULT TO ACTIVATE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL #305916, LOT #UNKNOWN. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. I WOULD LIKE TO BRING TO YOUR ATTENTION AN IMPORTANT SAFETY CONCERN REGARDING RECENT ORDER OF 25 G 1-INCH NEEDLES. WE HAVE OBSERVED THAT THESE NEEDLES ARE DIFFICULT TO ACTIVATE THE SAFETY LOCK AFTER THE INJECTION (THE SAFETY LOCK IS HARD TO PUSH UP AND BENDS THE NEEDLE), WHICH POSES A SIGNIFICANT SAFETY RISK. THIS ESPECIALLY CONCERNING IN THE PEDIATRIC CLINIC, WHERE A HIGH VOLUME OF VACCINES ARE ADMINISTERED DAILY. PEDIATRIC PATIENTS OFTEN MOVE UNEXPECTEDLY DURING OR AFTER AN INJECTION, INCREASING THE LIKELIHOOD OF ACCIDENTAL NEEDLE-STICK INJURIES WHEN IT'S DIFFICULT TO ACTIVATE THE SAFETY LOCK FOR SAFETY OF BOTH OUR STAFF AND PATIENTS, I KINDLY ASK YOU TO RECONSIDER THE USE OF THIS SPECIFIC NEEDLE AND EXPLORE ALTERNATIVE OPTIONS THAT ARE EASIER TO HANDLE POST-INJECTION. (B)(6): I AM FOLLOWING UP ON THE CONCERN RAISED BY SOME OF OUR (B)(6) STAFF ABOUT THE NEW 25G SAFETYGLIDE NEEDLES. I HAVE HAD AN OPPORTUNITY TO SPEAK WITH VARIOUS STAFF DURING RECEN

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23974060 ↗
• MalfunctionJan 6, 2026Activation Problem

  MDR (B)(4) WAS FILED IN ERROR.

  Patient problems: Needle Stick/Puncture

  MAUDE report 23974059 ↗
• MalfunctionDec 31, 2025Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23938150 ↗
• MalfunctionDec 31, 2025Break; Break

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23938144 ↗
• MalfunctionDec 25, 2025Break; Break

  IT WAS REPORTED THAT BD NEEDLE SFTYGLD 25X1 RB SAFETY MECHANISM BROKE IT WAS REPORTED BY CUSTOMER THAT THE SAFETY BROKE OFF COMPLETELY, LEAVING EXPOSED NEEDLE RCC RECEIVED A COMPLAINT VIA EMAIL. INCIDENT OR PROBLEM INFORMATION MDIP REFERENCE NUMBER (ID): 11858 DATES OF INCIDENT (YYYY-MM-DD): (B)(6) 2025 TYPE OF INCIDENT/PROBLEM: A2. FAILURE (I.E. WHILE PREPARING FOR, IN USE, AFTER USE) LEVEL OF HARM: OPTIONAL REPORT TO CMDSNET (HEALTH CANADA): INCIDENT DETAILS: I IMMUNIZED CLIENT, ATTEMPTED TO FLIP SAFETY ON SYRINGE. SAFETY BROKE OFF COMPLETELY, LEAVING EXPOSED NEEDLE. I WAS ABLE TO GET EXPOSED NEEDLE SAFELY TO SHARPS BIN WITHOUT INCIDENT. IMPACT OF INCIDENT: WHO WAS AFFECTED? UNEXPECTED OR PROLONGED CARE? YES DEVICE INFORMATION DEVICE NAME/DESCRIPTION: NEEDLE HYPODERMIC SAFETY 25GA X 1 IN MANUFACTURER: BECTON DICKINSON CANADA INC MANUFACTURER CODE/MODEL: 305916 SERIAL OR LOT NUMBER: (B)(6) EXPIRY DATE: 2027-09-30 SUPPLIER: (B)(4)/CATALOGUE NUMBER: 308-305916 IS THE DEVICE RETAINED? YES NUMBER OF DEVICES: 1 WIPED, CONTAINED, LABELLED? UNKNOWN DEVICE HANDLING HAZARDS (WHEN BLANK = HAZARDS NOT SPECIFIED).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23892566 ↗
• MalfunctionDec 15, 2025Break; Leak/Splash; Break; Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23811352 ↗

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