ARROW IPN915614Recalls & reported problems

Summary

The FDA's MAUDE database contains 48 adverse event reports that list this exact device (DI 10801902161243), received between Jun 28, 2023 and Sep 29, 2026 — classified as 1 injury, 47 malfunctions.

The most frequently reported specific device problem is “Crack” (16 reports).

1 FDA recall record name this device's identifier, 1 still open.

54 other recalls cover devices cleared under the same FDA submission (K071538); 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.

Recalls naming this device

1. Apr 21, 2026Open, Classified

   Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

   Z-2384-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 48 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Fluid/Blood Leak; Gas/Air Leak

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50932809 ↗
• MalfunctionJul 8, 2026Device Damaged Prior to Use; Material Twisted/Bent

  IT WAS REPORTED THAT A SMALL DEFECT WAS OBSERVED ON THE J-TIP OF THE GUIDEWIRE. THE GUIDEWIRE WAS NOT USED ON A PATIENT; THE ISSUE WAS IDENTIFIED WHILE A HEALTHCARE PROVIDER WAS PRACTICING WITH THE DEVICE IN A SIMULATION (SIM) TRAINING LABORATORY. THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THIS EVENT. NO ADVERSE PATIENT IMPACT, INJURY, OR HEALTH CONSEQUENCES OCCURRED, AND NO MEDICAL INTERVENTION WAS REQUIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25749727 ↗
• InjuryJun 9, 2026Material Separation; Unraveled Material; Physical Resistance/Sticking

  IT WAS REPORTED THAT THE SPRING WIRE GUIDE (SWG) ADVANCED SMOOTHLY THROUGH THE INTRODUCER NEEDLE AND THE INSERTION PROCEDURE WAS INITIALLY UNEVENTFUL. HOWEVER, RESISTANCE WAS ENCOUNTERED WHEN THE PHYSICIAN ATTEMPTED TO WITHDRAW THE SWG. UPON REMOVAL, THE SWG WAS OBSERVED TO BE FRAYED AND SUBSEQUENTLY BROKE, RESULTING IN A PORTION OF THE GUIDE WIRE REMAINING IN THE PATIENT'S LEG. THE PATIENT WAS TRANSFERRED TO INTERVENTIONAL RADIOLOGY, WHERE THE RETAINED FRAGMENT WAS SUCCESSFULLY RETRIEVED USING A SNARE WITHOUT COMPLICATION. THE PROCEDURE WAS ULTIMATELY COMPLETED SUCCESSFULLY, AND THE PATIENT'S CURRENT CONDITION WAS REPORTED AS "FINE". NO ADDITIONAL ADVERSE HEALTH CONSEQUENCES WERE REPORTED.

  Patient problems: Foreign Body In Patient

  MAUDE report 25446264 ↗
• MalfunctionMay 26, 2026Unraveled Material

  IT WAS REPORTED THAT THE SPRING WIRE GUIDE (SWG) WAS OBSERVED TO BE FRAYED (UNRAVELED) AND SUBSEQUENTLY CAME APART WHILE WITHIN THE PATIENT. THE PHYSICIAN LATER REPORTED THAT THERE WERE NO DIFFICULTIES ENCOUNTERED DURING REMOVAL OF THE SWG FROM THE VESSEL. THERE WERE NO REPORTS OF PATIENT INJURY, HARM, OR ADVERSE HEALTH CONSEQUENCES ASSOCIATED WITH THIS EVENT. THE PATIENT'S CONDITION WAS REPORTED AS "STABLE." NO ADDITIONAL MEDICAL OR SURGICAL INTERVENTION WAS REQUIRED BEYOND REMOVAL OF THE AFFECTED DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25283959 ↗
• MalfunctionMay 11, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT "DURING A CENTRAL LINE PLACEMENT UNDER ULTRASOUND GUIDANCE IN THE RIGHT FEMORAL VEIN, THE CLINICIAN OBSERVED BLOOD LEAKING FROM THE HUB OF THE INTRODUCER NEEDLE DURING ASPIRATION. THE PROCEDURE WAS SUCCESSFULLY COMPLETED USING AN ALTERNATE NEEDLE FROM THE KIT." THERE WERE NO REPORTS OF PATIENT INJURY, HARM, ADVERSE HEALTH CONSEQUENCES, OR MEDICAL INTERVENTION ASSOCIATED WITH THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25142254 ↗
• MalfunctionMay 11, 2026Crack; Fluid/Blood Leak

  IT WAS REPORTED THAT "DURING A CENTRAL LINE PLACEMENT, THE CLINICIAN OBSERVED BLOOD LEAKING FROM THE HUB OF THE INTRODUCER NEEDLE DURING ASPIRATION. THE PROCEDURE WAS STOPPED AND WAS SUCCESSFULLY COMPLETED USING AN ALTERNATE NEEDLE FROM THE KIT. IT WAS LATER CONFIRMED THAT THERE HAVE BEEN PREVIOUS REPORTS OF CRACKED HUBS ON INTRODUCER NEEDLES WITH THIS KIT." GOOD FAITH EFFORTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE REPORTED DEVICE ISSUES, INCLUDING CONFIRMATION OF THE MULTIPLE REPORTED OCCURRENCES AND ASSESSMENT OF ANY PATIENT HARM. THERE WERE DOCUMENTED ATTEMPTS MADE TO CONTACT THE USER FACILITY; HOWEVER, NO RESPONSE OR ADDITIONAL INFORMATION WAS RECEIVED. ASSOCIATED MDRS INCLUDE (SPECIFIC EVENT) AND 9680794-2026-00379 (MULTIPLE EVENTS WITHOUT ADDITIONAL DETAILS).

  Patient problems: Insufficient Information

  MAUDE report 25142111 ↗
• MalfunctionMay 8, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT, "DURING A CENTRAL LINE PLACEMENT, THE CLINICIAN OBSERVED BLOOD LEAKING FROM THE HUB OF THE NEEDLE DURING ASPIRATION. THE PROCEDURE WAS SUCCESSFULLY COMPLETED USING AN ALTERNATE NEEDLE FROM THE KIT." GOOD FAITH EFFORTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE REPORTED DEVICE ISSUE AND TO ASSESS WHETHER ANY PATIENT HARM, INJURY, OR ADVERSE HEALTH CONSEQUENCES OCCURRED. A TOTAL OF THREE DOCUMENTED ATTEMPTS WERE MADE TO CONTACT THE DISTRIBUTOR; HOWEVER, NO RESPONSE OR ADDITIONAL INFORMATION WAS RECEIVED.

  Patient problems: Insufficient Information

  MAUDE report 25127414 ↗
• MalfunctionMay 5, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT ON (B)(6) 2026, "THE OPERATING PHYSICIAN ACCESSED THE VEIN UNDER ULTRASOUND WITH THE INTRODUCER NEEDLE, BUT WHEN ATTEMPTING TO PULL BACK BLOOD, AIR WAS PULLED. NO HARM TO THE PATIENT AND THE PROCEDURE WAS COMPLETED BY A SECOND PUNCTURE FROM A SECOND KIT." THERE WERE NO REPORTS OF PATIENT INJURY, ADVERSE HEALTH CONSEQUENCES, OR MEDICAL INTERVENTIONS ASSOCIATED WITH THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25081495 ↗
• MalfunctionMay 5, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT, "THE OPERATING NURSE PRACTITIONER ACCESSED THE VEIN UNDER ULTRASOUND WITH THE INTRODUCER NEEDLE, BUT WHEN ATTEMPTING TO PULL BACK BLOOD, AIR WAS PULLED." THERE WERE NO REPORTS OF PATIENT INJURY, HARM, OR ADVERSE HEALTH CONSEQUENCES ASSOCIATED WITH THE EVENT. THE PATIENT'S CONDITION WAS REPORTED AS FINE. NO MEDICAL INTERVENTION WAS NECESSARY, AND THE PROCEDURE WAS COMPLETED AFTER CHANGING TO ANOTHER DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25081352 ↗
• MalfunctionApr 22, 2026Gas/Air Leak

  IT WAS REPORTED THAT "THE INTRODUCER NEEDLE WOULD NOT DRAW UP BLOOD WITH ASPIRATION, THE PROVIDER KEPT GETTING AIR BUBBLES. THE NEEDLE DID NOT APPEAR BROKEN OR BENT BUT WOULD NOT DRAW APPROPRIATELY PER THE PROVIDER AND REGISTERED NURSE." THERE WAS NO REPORT OF PATIENT HARM OR MEDICAL INTERVENTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24958785 ↗
• MalfunctionApr 14, 2026Leak/Splash

  IT WAS REPORTED "INTRODUCER NEEDLE LEAKING DURING USE". THE USER CHANGED TO A NEW SET TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24871948 ↗
• MalfunctionApr 3, 2026Fluid/Blood Leak; Failure to Seal

  IT WAS REPORTED "MD PLACING CVC CATHETER INTO FEMORAL ARTERY WHEN INTRODUCER CATHETER WITH SYRINGE WOULD NOT DRAW BACK. ANOTHER 2 KITS FROM NEURO ICU AND ICU WERE USED WITH THE SAME ISSUE. UNABLE TO DRAW BACK BLOOD OR NOT A CLOSED SEAL AND BLOOD WOULD LEAK OUT OF THE SYRINGE." ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "UNKNOWN". ASSOCIATE MDR NUMBERS INCLUDE: 9680794-2026-00243, 9680794-2026-00242, AND 9680794-2026-00241.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24777510 ↗
• MalfunctionApr 3, 2026Failure to Seal

  IT WAS REPORTED "MD PLACING CVC CATHETER INTO FEMORAL ARTERY WHEN INTRODUCER CATHETER WITH SYRINGE WOULD NOT DRAW BACK. ANOTHER 2 KITS FROM NEURO ICU AND ICU WERE USED WITH THE SAME ISSUE. UNABLE TO DRAW BACK BLOOD OR NOT A CLOSED SEAL AND BLOOD WOULD LEAK OUT OF THE SYRINGE." ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "UNKNOWN". ASSOCIATE MDR NUMBERS INCLUDE: 9680794-2026-00243, AND 9680794-2026-00241.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24777187 ↗
• MalfunctionApr 3, 2026Failure to Seal

  IT WAS REPORTED "MD PLACING CVC CATHETER INTO FEMORAL ARTERY WHEN INTRODUCER CATHETER WITH SYRINGE WOULD NOT DRAW BACK. ANOTHER 2 KITS FROM NEURO ICU AND ICU WERE USED WITH THE SAME ISSUE. UNABLE TO DRAW BACK BLOOD OR NOT A CLOSED SEAL AND BLOOD WOULD LEAK OUT OF THE SYRINGE." ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "UNKNOWN". ASSOCIATE MDR NUMBERS INCLUDE: 9680794-2026-00242, AND 9680794-2026-00241.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24777151 ↗
• MalfunctionApr 3, 2026Crack

  IT WAS REPORTED "BOTH NEEDLES IN RAULERSON SYRINGE WERE CRACKED AND UNABLE TO USE". THIS WAS FOUND PRIOR TO USE. BOTH KITS WERE USED ON THE SAME PATIENT. A THIRD KIT WAS USED SUCCESSFULLY. THERE WAS NO PATIENT INVOLVEMENT. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE". ASSOCIATE MDR NUMBERS INCLUDE: 9680794-2026-00235.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24775857 ↗
• MalfunctionApr 3, 2026Crack

  IT WAS REPORTED "BOTH NEEDLES IN RAULERSON SYRINGE WERE CRACKED AND UNABLE TO USE". THIS WAS FOUND PRIOR TO USE. BOTH KITS WERE USED ON THE SAME PATIENT. A THIRD KIT WAS USED SUCCESSFULLY. THERE WAS NO PATIENT INVOLVEMENT. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE". ASSOCIATE MDR NUMBERS INCLUDE: 9680794-2026-00234.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24775807 ↗
• MalfunctionMar 18, 2026Break

  IT WAS REPORTED "INTRODUCER NEEDLE IN THE KIT HAS A BROKEN HUB". THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24634677 ↗
• MalfunctionMar 18, 2026Break

  IT WAS REPORTED "INTRODUCER NEEDLE IN THE KIT HAS A BROKEN HUB". THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24626915 ↗
• MalfunctionMar 18, 2026Crack; Suction Failure

  IT WAS REPORTED THAT "PER THE CHARGE NURSE AND THE RESIDENT PHYSICIANS THEY STATED THAT THE SYRINGE THAT USED TO CHECK FOR LINE PLACEMENT BY ASPIRATING FOR BLOOD IN TWO SEPARATE KITS WERE DEFECTIVE. THE SPECIFIC KITS WERE THE TRIPLE LUMEN CVC LINE, IN ONE OF THE KITS THE SYRINGE WAS VISIBLE CRACKED AND WHEN THEY ATTEMPTED TO ASPIRATE BLOOD, IT LEAKED OUT OF THE CRACK AND IN THE OTHER KIT THE SYRINGE DID HAVE NOT SUCTION AND WOULD NOT ASPIRATE AND THEY WERE UNABLE TO CHECK FOR PLACEMENT. "THE PHYSICIAN WAS ATTEMPTING TO PLACE A CENTRAL LINE LAST NIGHT AND YET AGAIN WHEN ATTEMPTING TO CHECK PLACEMENT, THE SYRINGE PROVIDED IN THE KIT DID NOT HAVE ANY SUCTION AND THEY COULD NOT ASPIRATE ANY BLOOD . THEY HAD TO GET ANOTHER SYRINGE AND THAT SYRINGE WORKED CORRECTLY." THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE". ASSOCIATED MDR NUMBERS INCLUDE: 9680794-2026-00212, 9680794-2026-00211, AND 9680794-2026-00210.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24626738 ↗
• MalfunctionMar 17, 2026Crack

  IT WAS REPORTED "WHILE GAINING ACCESS TO THE PATIENT'S VESSEL, IT WAS OBSERVED THAT PLASTIC HUB OF THE 18GA X 2.5" NEEDLE CRACKED. FROM CUSTOMER 'PLACED AND THE CONNECTION PIECE ON THE PUNCTURE NEEDLE FOR THE INTRODUCER SYRINGE CRACKED'." THERE WAS NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "CRITICAL". THE PATIENT WAS CRITICAL PRIOR TO THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24616720 ↗
• MalfunctionMar 11, 2026Leak/Splash; No Pressure

  IT WAS REPORTED THAT "FAULTY INTRODUCER NEEDLE IN KIT". ADDITIONAL INFORMATION RECEIVED STATES "WHEN TRYING TO ASPIRATE AFTER ACCESSING THE VESSEL THE SYRINGE WOULD NOT CREATE ANY NEGATIVE PRESSURE, WAS PULLING IN AIR. INSERTER WAS POSITIVE THEY WERE IN THE VESSEL." A NEW DEVICE WAS USED. THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS UNKNOWN AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24574458 ↗
• MalfunctionMar 11, 2026Crack; Leak/Splash

  IT WAS REPORTED THAT "DURING CENTRAL LINE PLACEMENT, INTRODUCER NEEDLE WAS INSERTED UNDER US GUIDANCE. WHEN I WENT TO PULLBACK ON THE SYRINGE, I GOT AIR BUBBLES MIXED WITH BLOOD RETURN. AFTER REMOVING THE NEEDLE, ATTEMPTED TO FLUSH THE NEEDLE AND THE SYRINGE WITH NORMAL SALINE. I HAD A SIMILAR FINDING, WITH AIR BUBBLES IN THE SYRINGE. WHEN FLUSHING THE SALINE OUT, FLUID WAS EXPELLED OUT THE SIDE OF THE NEEDLE HUB, REVEALING A HOLE WITHIN THE NEEDLE HUB THAT COULD INAPPROPRIATELY INTRODUCE AIR INTO THE CLOSED SYSTEM. THE NEEDLE WAS DISCARDED AND A NEW CVC KIT WAS OPENED. PROCEDURE WAS COMPLETED WITH NO COMPLICATIONS TO THE PATIENT." THERE WAS NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24568351 ↗
• MalfunctionMar 10, 2026Crack; Gas/Air Leak

  IT WAS REPORTED THAT "WE HAD 2 WITH CRACKED HUBS PULLING IN AIR". THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS UNKNOWN AT THIS TIME. ASSOCIATE MDR NUMBERS INCLUDE:9680794-2026-00168 AND 9680794-2026-00167.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24559337 ↗
• MalfunctionMar 10, 2026Crack; Gas/Air Leak

  IT WAS REPORTED THAT "WE HAD 2 WITH CRACKED HUBS PULLING IN AIR". THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS UNKNOWN AT THIS TIME. ASSOCIATE MDR NUMBERS INCLUDE:9680794-2026-00168 AND 9680794-2026-00167.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24559322 ↗
• MalfunctionMar 9, 2026Crack

  IT WAS REPORTED THAT "DURING PROCEDURE THE MD ATTEMPTED TO DRAW BACK ON ASPIRATION NEEDLE/SYRINGE WITH NO BLOOD RETURN DESPITE US VERIFICATION. MD VERIFIED THERE WAS A CRACK IN THE SYRINGE". THE DEVICE WAS REMOVED AND REPLACED. THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24547023 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071538. One submission often covers many models, so check the product and lot details in each record.

• Z-2376-2026 · Apr 21, 2026 · Open, Classified
  Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-
• Z-1914-2026 · Mar 11, 2026 · Open, Classified
  ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-4
• Z-2123-2026 · Jan 7, 2026 · Open, Classified
  Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
• Z-0003-2024 · Aug 10, 2023 · Open, Classified
  Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
• Z-0002-2024 · Aug 10, 2023 · Open, Classified
  Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
• Z-0351-2023 · Oct 27, 2022 · Terminated
  Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
• Z-0352-2023 · Oct 27, 2022 · Terminated
  Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-
• Z-1604-2022 · May 25, 2022 · Open, Classified
  TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)
• Z-1988-2018 · Apr 11, 2018 · Terminated
  Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Codes: ASK-42703-PAM1, ASK-42703-PSHR1, ASK-45703-PNY, ASK-45703-PWHC1
• Z-1996-2018 · Apr 11, 2018 · Terminated
  Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; P
• Z-1997-2018 · Apr 11, 2018 · Terminated
  Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-PTJH
• Z-1999-2018 · Apr 11, 2018 · Terminated
  Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-427
• Z-1990-2018 · Apr 11, 2018 · Terminated
  Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Code: ASK-45802-PHMW
• Z-1987-2018 · Apr 11, 2018 · Terminated
  Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1
• Z-1979-2018 · Apr 11, 2018 · Terminated
  Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-15703-LD

…and 39 more.