ARROW IPN030935Recalls & reported problems

Summary

The FDA's MAUDE database contains 34 adverse event reports that list this exact device (DI 10801902029390), received between Jun 21, 2023 and Mar 25, 2026 — classified as 34 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (8 reports).

12 other recalls cover devices cleared under the same FDA submission (K900263); 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 34 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 25, 2026Material Twisted/Bent

  IT WAS REPORTED THAT "PATIENT WITH INDICATION FOR TRIPLE-LUMEN CENTRAL VENOUS CATHETER INSERTION. DURING THE PROCEDURE, WHILE ADVANCING THE DILATOR, IT FAILED TO ENTER THE PUNCTURE SITE PROPERLY DUE TO KINKING/BENDING". ANOTHER CATHETER WAS USED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "DECEASED". SEVERAL ATTEMPTS WERE MADE TO GET ADDITIONAL INFORMATION FROM THE CUSTOMER; HOWEVER, FURTHER DETAILS HAVE NOT BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24688054 ↗
• MalfunctionMar 23, 2026Material Deformation

  IT WAS REPORTED THAT "THE CENTRAL VENOUS CATHETER (CVC) DILATOR TIP WAS DEFECTIVE. DURING INSERTION, IT WAS DIFFICULT TO CANNULATE THE VEIN". ANOTHER DEVICE WAS USED. 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 24662102 ↗
• MalfunctionMar 19, 2026Material Twisted/Bent

  IT WAS REPORTED THAT "WHILE DILATING WITH ARROW BRAND CVC EQUIPMENT AND ADVANCING THE CATHETER, A BENT SELDINGER GUIDE WAS FOUND, SO IT HAD TO BE REMOVED." THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS DISCHARGED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24638730 ↗
• MalfunctionFeb 9, 2026Material Deformation

  IT WAS REPORTED THAT "A SINGLE PUNCTURE IS PERFORMED IN THE LEFT INFRACLAVICULAR REGION UNTIL VENOUS RETURN IS OBTAINED. THE METAL GUIDE IS ADVANCED EASILY, FOLLOWED BY THE DILATOR AND THEN THE CATHETER. WHEN ATTEMPTING TO RETRIEVE THE GUIDE, DEFORMATION OF THE GUIDE IS OBSERVED, SO IT IS DECIDED TO COMPLETELY REMOVE THE CATHETER. A SECOND CATHETER IS REQUESTED AND THE PROCEDURE IS REPEATED: SINGLE PUNCTURE IN THE LEFT INFRACLAVICULAR REGION UNTIL VENOUS RETURN IS OBTAINED, METAL GUIDE ADVANCED EASILY, ADVANCEMENT OF THE DILATOR AND CATHETER. THEN, THE METAL GUIDE IS RETRIEVED, THE CATHETER IS FIXED AT 18 CM, AND THE LINES ARE TESTED AND FLUSHED." 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 24290750 ↗
• MalfunctionFeb 4, 2026Material Frayed

  IT WAS REPORTED THAT "A TRIPLE-LUMEN CENTRAL VENOUS CATHETER, INVOLVING AN ONCOLOGY PATIENT IN WHOM THE FIRST STEP OF GUIDEWIRE AND CATHETER PLACEMENT WAS PERFORMED. AT THE TIME OF GUIDEWIRE REMOVAL, THE ATTENDING PHYSICIAN OBSERVED AN ABNORMALITY, NOTING A FRAYED APPEARANCE, ALTHOUGH THE GUIDEWIRE WAS REMOVED IN ITS ENTIRETY. SUBSEQUENTLY, A SECOND ATTEMPT WAS MADE TO PLACE THE CATHETER AND GUIDEWIRE USING THE SELDINGER TECHNIQUE; DURING THE REMOVAL OF THE GUIDEWIRE, THE SAME FRAYING PHENOMENON OCCURRED, WITH THE PARTICULARITY THAT THE GUIDEWIRE BECAME LODGED IN THE PATIENT'S ACCESS SITE. AS A RESULT, THE PATIENT REQUIRED SURGICAL INTERVENTION FOR DEVICE REMOVAL." THE PATIENT'S CURRENT CONDITION IS REPORTED AS "DECEASED". IT WAS REPORTED "THE DEVICE DID NOT POTENTIALLY CONTRIBUTE TO THE PATIENTS DEATH". ASSOCIATED MDR NUMBERS INCLUDE: 3006425876-2026-00088.

  Patient problems: Insufficient Information

  MAUDE report 24257225 ↗
• MalfunctionJul 28, 2025Obstruction of Flow; Improper Flow or Infusion; Obstruction of Flow; Improper Flow or Infusion

  IT WAS REPORTED "CATHETER DOES NOT REFLOW OR INFUSE ONCE INSTALLED BY AN INTENSIVIST." THE CATHETER WAS REMOVED AND REPLACED SUCCESSFULLY. 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 22629182 ↗
• MalfunctionJul 9, 2025Fracture; Fracture

  IT WAS REPORTED "PATIENT WITH DIFFICULT VENOUS ACCESS FOR WHOM A CENTRAL VENOUS CATHETER (CVC) PLACEMENT WAS INDICATED. UPON UNPACKING THE DEVICE, NO APPARENT DAMAGE WAS OBSERVED. DURING RIGHT SUBCLAVIAN VEIN PUNCTURE BY THE INTENSIVIST, NEEDLE FRACTURE OCCURRED. A NEW CVC WAS REQUESTED, WITH SUCCESSFUL PLACEMENT VIA LEFT JUGULAR ACCESS USING STERILE TECHNIQUE AND NO IMMEDIATE COMPLICATIONS PROCESSES AND INVENTORY MANAGEMENT COMPLICATIONS." THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "REFERRED TO ANOTHER CLINIC".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22457118 ↗
• MalfunctionJun 16, 2025Device Damaged Prior to Use; Device Damaged Prior to Use

  IT WAS REPORTED "PATIENT REQUIRING CENTRAL CATHETER INSERTION FOR MULTIPLE INFUSION ADMINISTRATION; PHYSICIAN ON DUTY OPENS THE CATHETER, WHEN THE GUIDEWIRE IS CHECKED IT IS DAMAGED, A NEW DEVICE ORDER IS PLACED." THIS WAS FOUND PRIOR TO USE. 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 22210279 ↗
• MalfunctionMay 7, 2025Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED "INTENSIVIST ON DUTY, DOCTOR PROCEEDS TO PERFORM THE INSERTION, PUNCTURE THE PATIENT IS EVIDENCE RETURN AND PROGRESS OF THE GUIDE AND AT THE TIME OF TO TAKE OUT THE GUIDE, IT IS EVIDENT THAT THE COATING OF THE GUIDE, CAUSING DIFFICULTY IN THE REMOVAL OF IT, GENERATING PAIN TO THE PATIENT AND SUBSEQUENT COMPLICATIONS, IT IS AC HIEVED REMOVE THE GUIDEWIRE AND ADVANCE CATHETER, BUT IT IS NOT EVIDENCE RETURN, THE CATHETER IS FOUND DYSFUNCTIONAL, LUMENS ARE TESTED BUT NOT HE GETS NO RETURN, FOR THIS REASON THE DOCTOR IN TURN, HE REMOVES A CATHETER AND DECIDES TO PLACE ANOTHER ONE." THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE". ASSOCIATED MDR NUMBERS INCLUDE: 3006425876-2025-00433.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21977106 ↗
• MalfunctionMay 7, 2025Difficult to Remove; Physical Resistance/Sticking; Difficult to Remove; Physical Resistance/Sticking

  IT WAS REPORTED "INTENSIVIST ON DUTY, DOCTOR PROCEEDS TO PERFORM THE INSERTION, PUNCTURE THE PATIENT IS EVIDENCE RETURN AND PROGRESS OF THE GUIDE AND AT THE TIME OF TO TAKE OUT THE GUIDE, IT IS EVIDENT THAT THE COATING OF THE GUIDE, CAUSING DIFFICULTY IN THE REMOVAL OF IT, GENERATING PAIN TO THE PATIENT AND SUBSEQUENT COMPLICATIONS, IT IS ACHIEVED REMOVE THE GUIDEWIRE AND ADVANCE CATHETER, BUT IT IS NOT EVIDENCE RETURN, THE CATHETER IS FOUND DYSFUNCTIONAL, LUMENS ARE TESTED BUT NOT HE GETS NO RETURN, FOR THIS REASON THE DOCTOR IN TURN, HE REMOVES A CATHETER AND DECIDES TO PLACE ANOTHER ONE." THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE". ASSOCIATED MDR NUMBERS INCLUDE: 3006425876-2025-00433 AND 3006425876-2025-00447.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21975780 ↗
• MalfunctionMar 27, 2025Positioning Failure; Positioning Failure

  IT WAS REPORTED "A 14-YEAR-OLD FEMALE PATIENT WITH A DIAGNOSIS OF SEVERE PREECLAMPSIA REQUIRED CENTRAL VENOUS ACCESS IN THE RIGHT SUBCLAVIAN ARTERY. DURING INSERTION, WHEN THE GUIDEWIRE WAS REMOVED, IT WAS OBSERVED THAT IT CAME OUT IN A SPIRAL SHAPE (THE RESORTED MATERIAL COVERING THE GUIDEWIRE WAS PARTIALLY SEPARATED AND STRETCHED). A PORTABLE CHEST X-RAY WAS PERFORMED, SHOWING THAT THE CATHETER WAS NOT IN THE RIGHT POSITION, NO HEMOTHORAX OR PNEUMOTHORAX WAS OBSERVED. A NEW CENTRAL VENOUS CATHETER WAS USED, WITHOUT ANY OTHER COMPLICATIONS.". THE ASSOCIATED EMDR REPORT NUMBERS ARE 3006425876-2025-00324 AND 3006425876-2025-00312.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21706399 ↗
• MalfunctionMar 27, 2025Unraveled Material; Unraveled Material

  IT WAS REPORTED "A 14-YEAR-OLD FEMALE PATIENT WITH A DIAGNOSIS OF SEVERE PREECLAMPSIA REQUIRED CENTRAL VENOUS ACCESS IN THE RIGHT SUBCLAVIAN ARTERY. DURING INSERTION, WHEN THE GUIDEWIRE WAS REMOVED, IT WAS OBSERVED THAT IT CAME OUT IN A SPIRAL SHAPE (THE RESORTED MATERIAL COVERING THE GUIDEWIRE WAS PARTIALLY SEPARATED AND STRETCHED). A PORTABLE CHEST X-RAY WAS PERFORMED, SHOWING THAT THE CATHETER WAS NOT IN THE RIGHT POSITION, NO HEMOTHORAX OR PNEUMOTHORAX WAS OBSERVED. A NEW CENTRAL VENOUS CATHETER WAS USED, WITHOUT ANY OTHER COMPLICATIONS.". THE ASSOCIATED EMDR REPORT NUMBERS ARE 3006425876-2025-00324 .

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21706385 ↗
• MalfunctionMar 18, 2025Difficult to Advance; Difficult to Advance

  IT WAS REPORTED THAT DURING A MAJOR SURGERY, A PATIENT IN A STATE OF DEEP ANESTHESIA REQUIRED A CENTRAL VENOUS CATHETER. MULTIPLE ATTEMPTS WERE MADE BY BOTH THE ANESTHESIOLOGIST AND THE SURGICAL ONCOLOGIST; HOWEVER, THE GUIDEWIRE DID NOT PASS EASILY, AND THE DILATOR FAILED TO DILATE AS EXPECTED. THE PATIENT HAD NO HARM OR INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21630823 ↗
• MalfunctionMar 12, 2025Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT A PATIENT REQUIRING INVASIVE ACCESS FOR SURGERY AND MEDICATION ADMINISTRATION UNDERWENT AN ATTEMPTED RIGHT JUGULAR CENTRAL CATHETER PLACEMENT BY THE ANAESTHESIOLOGIST. HOWEVER, UPON PUNCTURE AND GUIDE INSERTION, THE GUIDE DID NOT PASS AND INSTEAD BENT. THE PATIENT HAD NO HARM OR INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21584940 ↗
• MalfunctionMar 12, 2025Material Rupture; Material Rupture

  IT WAS REPORTED THAT "THE CATHETER COMES OUT IN THE MEDIAL AND DISTAL LINE WITH A RUPTURE NEAR THE JUNCTION OF THE LINES, IT IS EVIDENT WHEN STARTING TO USE THE DEVICE SINCE LIQUID COMES OUT WHEN ADMINISTERED." THE PATIENT HAD NO HARM OR INJURY. THE ASSOCIATED EMDR REPORT NUMBERS ARE 3006425876-2025-00299.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21584924 ↗
• MalfunctionMar 12, 2025Material Rupture; Material Rupture

  IT WAS REPORTED THAT "THE CATHETER COMES OUT IN THE MEDIAL AND DISTAL LINE WITH A RUPTURE NEAR THE JUNCTION OF THE LINES, IT IS EVIDENT WHEN STARTING TO USE THE DEVICE SINCE LIQUID COMES OUT WHEN ADMINISTERED.". THE PATIENT HAD NO HARM OR INJURY. THE ASSOCIATED EMDR REPORT NUMBERS ARE 3006425876-2025-00299 AND 3006425876-2025-00298.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21584915 ↗
• MalfunctionFeb 12, 2025Material Protrusion/Extrusion; Material Protrusion/Extrusion

  IT WAS REPORTED THAT "CENTRAL VENOUS CATHETER 7 FR IS OBSERVED TO HAVE BULGING IN THE MEDIAL LUMEN, WHICH IMPRESSES THE HEALTH TEAM. THE CENTRAL LINE IS CHANGED". THE PATIENT HAD NO HARM OR INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21364387 ↗
• MalfunctionJul 15, 2024Unraveled Material; Unraveled Material

  IT WAS REPORTED "A 7FR TRI-LUMEN PICC CATHETER IS USED AND THIS PROCESS IS PERFORMED BY AN INTENSIVE CARE PHYSICIAN IN THE INTENSIVE CARE UNIT AND WITH THE USE OF ULTRASOUND GUIDANCE TO VERIFY VASCULAR ACCESS. ONCE THE VEIN IS CANALIZED, THE METAL GUIDE IS PASSED, AND WHEN THE GUIDE IS REMOVED IT IS OBSERVED HOW IT IS COMING LOOSE, SO IT IS CAREFULLY REMOVED AND AT THE END IT IS BROKEN WITHOUT CAUSING HARM TO THE PATIENT. A NEW KIT IS USED TO COMPLETE THE PROCEDURE, WHICH IS SUCCESSFUL WITHOUT PROBLEMS." NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19742794 ↗
• MalfunctionJun 7, 2024Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT: "WHEN INTRODUCING THE GUIDE WIRE DURING SURGERY IT BENT AND HAD TO BE REMOVED. ANOTHER GUIDE WAS USED TO COMPLETE THE SURGERY. THERE WAS NO REPORTED PATIENT HARM OR CONSEQUENCE." ASSOCIATED COMPLAINTS 3006425876-2024-00492 AND 3006425876-2024-00492.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19489244 ↗
• MalfunctionJun 4, 2024Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED "IT DOES NOT COMPLETELY PASS THE GUIDE AND WHEN REMOVING OR POSITIONING THE MEMORY IS LOST AND IT IS NO LONGER USEFUL, IT CANNOT BE RE-ENTERED". 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 19460773 ↗
• MalfunctionJun 4, 2024Difficult to Advance; Difficult to Advance

  IT WAS REPORTED "IT DOES NOT COMPLETELY PASS THE GUIDE AND WHEN REMOVING OR POSITIONING THE MEMORY IS LOST AND IT IS NO LONGER USEFUL, IT CANNOT BE RE-ENTERED". 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 19460638 ↗
• MalfunctionMay 21, 2024Material Deformation; Physical Resistance/Sticking; Material Deformation; Physical Resistance/Sticking

  IT WAS REPORTED THAT: WHEN THE DOCTOR ATTEMPTED TO INSERT THE GUIDE WIRE IT BENT. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO REPORTED PATIENT HARM OR CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19357554 ↗
• MalfunctionMay 20, 2024Material Deformation; Physical Resistance/Sticking; Material Deformation; Physical Resistance/Sticking

  IT WAS REPORTED "SPECIALIST REFERS TO PERFORMING THE GUIDE STEP WHICH DID NOT PASS COMPLETELY; THEREFORE HE DECIDES TO REMOVE, AT THE MOMENT OF REMOVING IT IS EVIDENT THAT THE GUIDE IS SUFFERING DEFORMATION." ADDITIONAL INFORMATION REPORTS "THE GUIDE SUFFERS A STRETCHING MAKIN MANIPULATION IMPOSSIBLE". 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 19352996 ↗
• MalfunctionApr 8, 2024Deformation Due to Compressive Stress; Deformation Due to Compressive Stress

  IT WAS REPORTED THAT: WHEN CLINICIAN OPENED THE PACKAGE THE GUIDE WIRE WAS BENT. THE DEVICE WAS NOT USED ON PATIENT. THERE WAS NO REPORTED PATIENT HARM OR CONSEQUENCE.

  Patient problems: Insufficient Information

  MAUDE report 19059004 ↗
• MalfunctionApr 2, 2024Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED "THE GUIDEWIRE IS OBSERVED TO BE VERY FLEXIBLE AND THEREFORE DOES NOT ALLOW ITS USE IN THE PATIENT." ANOTHER DEVICE WAS SUCCESSFULLY USED. THIS DEFECT WAS FOUND PRIOR TO USE. THEREFORE, THERE WAS NO PATIENT HARM OR INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19021675 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K900263. 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-0053-2020 · May 17, 2019 · Terminated
  Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product Usage; Provide short-term (< 30 days) central venous acces
• Z-2886-2018 · Jul 3, 2018 · Terminated
  Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502 Product Usage: The multiple-lumen catheter permits venous acc
• Z-1985-2018 · Apr 11, 2018 · Terminated
  ARROWg+ard Blue(R) Central Venous Catheterization Kit; Product Code: ASK-24306-WHC1 and ASK-24306-WHC2
• Z-1984-2018 · Apr 11, 2018 · Terminated
  Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter and Sharps Safety Features; Product Code: ASK-24306-VC
• Z-1333-2018 · Dec 22, 2017 · Terminated
  ARROWg+ard Blue CVC Kit (1) Part Number (PN): CDC-24301-1A, (2) PN: CDC-24306-1A; (3) ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit, PN: CDC-22123-1A; (4) Central Venous Catheter
• Z-1001-2018 · Nov 27, 2017 · Terminated
  ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit Product Usage: The Arrow CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or condi
• Z-2337-2017 · May 9, 2017 · Terminated
  ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation
• Z-1830-2012 · May 3, 2012 · Terminated
  Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The multiple-lumen catheter permits venous access to central circ
• Z-2496-2010 · Jul 29, 2010 · Terminated
  Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter
• Z-1499-2009 · Feb 11, 2009 · Terminated
  Arrow ARROWg+ard CVCs (Central Venous Catheters)
• Z-0082-04 · Sep 16, 2003 · Terminated
  Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm