CLEARLINK/CONTINU-FLO 2R8546Recalls & reported problems

Summary

The FDA's MAUDE database contains 59 adverse event reports that list this exact device (DI 00085412565699), received between Apr 26, 2022 and Feb 25, 2026 — classified as 59 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (56 reports).

13 other recalls cover devices cleared under the same FDA submission (K180739, K961225); 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 59 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 25, 2026Crack; Detachment of Device or Device Component

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET HAD A CRACK OR BREAK IN AN UNSPECIFIED RIGID COMPONENT. ADDITIONALLY, IT WAS NOTED THAT THERE WAS A SEPARATION BETWEEN TWO BONDED COMPONENTS. THIS OCCURRED DURING PATIENT INFUSION IN A NEONATAL INTENSIVE CARE UNIT (NICU). THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24445119 ↗
• MalfunctionFeb 18, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON DEHP CONTINU FLO SOLUTION SET LEAKED PRIOR TO THE ANTI SIPHON VALVE DURING A TOTAL PARENTERAL NUTRITION(TPN) INFUSION. THE TPN WAS BEING INFUSED THROUGH A DUAL LUMEN INTERNAL JUGULAR LINE. THE TUBING SETUP WAS CHANGED TO RESOLVE THE ISSUE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24374824 ↗
• MalfunctionFeb 6, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED FROM THE GLAND OF THE Y-SITE (CLEARLINK) DESPITE PRESENCE OF GREEN ALCOHOL CAPS. THE FLUIDS WERE BEING INFUSED VIA PERIPHERAL INTRAVENOUS LINE (PIV). THE TUBING AND FLUIDS WERE REPLACED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24280299 ↗
• MalfunctionAug 14, 2025Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak

  IT WAS REPORTED THAT A STAIN WAS NOTICED BENEATH THE LINE OF A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET WHILE CHANGING LINENS. THE ISSUE OCCURRED DURING PATIENT INFUSION WITH LIPIDS. A BLUE CHUCKS PAD WAS PLACED UNDER THE PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) LINE TUBING AND WITHIN 2 MINUTES SHOWED LEAKING AT THE SITE OF LIPID FILTER/IV TUBING CONNECTION; A CRACK AT THE CONNECTION SIDE OF THE SOLUTION SET WAS NOTICED. THE LINE WAS CHANGED UNDER STERILE CONDITIONS TO RESOLVE THE ISSUE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22809595 ↗
• MalfunctionJul 14, 2025Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED EXCESSIVE AMOUNTS OF TOTAL PARENTERAL NUTRITION (TPN) FROM TWO DIFFERENT Y-SITE PORTS DESPITE PRESENCE OF NON-BAXTER GREEN ALCOHOL CAPS. THE ISSUE OCCURRED DURING PATIENT USE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22501301 ↗
• MalfunctionJun 9, 2025Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED FROM THE MIDDLE Y-SITE CONNECTION (PROTECTED BY A NON-BAXTER CAP). THE ISSUE OCCURRED DURING PATIENT INFUSION WITH TOTAL PARENTERAL NUTRITION (TPN) AND LIPIDS. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22172332 ↗
• MalfunctionMar 19, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  I WAS REPORTED THAT THE TUBING DISCONNECTED AT THE Y-PORT (CLEARLINK) OF A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET DURING PRIMING. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21642368 ↗
• MalfunctionMar 3, 2025Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED TOTAL PARENTERAL NUTRITION (TPN) FROM THE Y-SITE (CLEARLINK) AT A "BRISK RATE". THIS WAS OBSERVED DURING PATIENT USE. THE ISSUE WAS FURTHER DESCRIBED AS, "VISIBLE DRIP FROM 2ND Y SITE DOWN FROM THE SPIKE". NEW INTRAVENOUS FLUIDS WERE ORDERED TO RESOLVE THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21511188 ↗
• MalfunctionFeb 18, 2025Disconnection; Disconnection

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET DISCONNECTED FROM AN UNSPECIFIED LIPID FILTER. THIS WAS OBSERVED DURING INFUSION OF TOTAL PARENTERAL NUTRITION (TPN)/INTRALIPID (IL) VIA A PERIPHERALLY INSERTED CENTRAL CATHETER (PICC). THE IL BAG WAS RE-SPIKED STERILELY, NEW TUBING AND LIPID FILTER WERE PRIMED, AND NEW TUBING CONNECTED TO PICC LINE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21396999 ↗
• MalfunctionFeb 18, 2025Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET WAS LEAKING SMOF LIPIDS FROM THE TUBING. THE LEAK WAS DISCOVERED WITHIN THE NEONATAL ICU UNIT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21392600 ↗
• MalfunctionDec 27, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE DESPITE GREEN ALCOHOL CAP BEING IN PLACE DURING PATIENT INFUSION. THIS WAS OBSERVED DURING LINE AUDITS. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21030553 ↗
• MalfunctionDec 27, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE DESPITE GREEN ALCOHOL CAP BEING IN PLACE. THIS WAS NOTICED WHILE PERFORMING DAILY AUDITS. THE DEVICE CONTAINED TOTAL PARENTERAL NUTRITION (TPN). THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21027040 ↗
• MalfunctionDec 2, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE (CLEARLINK) DESPITE A NON-BAXTER GREEN ALCOHOL CAP BEING IN PLACE. THIS OCCURRED DURING PATIENT INFUSION WITH TOTAL PARENTERAL NUTRITION (TPN). NEW FLUIDS WOULD BE ORDERED AND THE SET REPLACED TO RESOLVE THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20827291 ↗
• MalfunctionNov 19, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED TOTAL PARENTERAL NUTRITION (TPN) AT THE Y-SITE (CLEARLINK) PORT WHILE A NON-BAXTER GREEN ALCOHOL CAP WAS IN PLACE. THIS OCCURRED DURING PATIENT USE. THE SET WOULD BE REPLACED TO RESOLVE THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20728773 ↗
• MalfunctionNov 19, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE PORT WHILE THE GREEN ALCOHOL CAP WAS IN PLACE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20725902 ↗
• MalfunctionNov 12, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED TOTAL PARENTERAL NUTRITION (TPN) FROM THE Y-SITE (CLEARLINK) DESPITE A NON-BAXTER GREEN ALCOHOL CAP BEING IN PLACE. THIS WAS OBSERVED DURING A DAILY AUDIT. CLEAR FLUIDS WOULD BE ORDERED AND THE LINE CHANGED TO RESOLVE THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20665948 ↗
• MalfunctionNov 8, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED FROM THE Y-SITE DESPITE GREEN ALCOHOL CAP BEING IN PLACE. THE LINE WAS TO BE CHANGED PER PROTOCOL. THIS WAS OBSERVED DURING AUDITS. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20646267 ↗
• MalfunctionNov 8, 2024Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak

  IT WAS REPORTED THAT THE TUBING OF A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED. THE ISSUE WAS FURTHER DESCRIBED AS, 'TUBING NOTED TO BE CRACKED BETWEEN MALE SITE AT END OF BAXTER TUBING AND FEMALE SITE AT START OF IL FILTER'. THIS WAS OBSERVED WHILE ASSESSING THE PATIENT'S LINE. TO RESOLVE THIS ISSUE, THE SET WAS CHANGED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20643451 ↗
• MalfunctionNov 8, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE PORT DESPITE HAVING A GREEN ALCOHOL CAP IN PLACE. THIS WAS OBSERVED DURING DAILY AUDITS. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20641877 ↗
• MalfunctionOct 23, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE (CLEARLINK). THE TPN (TOTAL PARENTERAL NUTRITION) LINE WAS LEAKING DESPITE GREEN ALCOHOL CAPS BEING IN PLACE. THIS WAS OBSERVED DURING CENTRAL LINE AUDITS. TO RESOLVE THE EVENT, CLEAR FLUIDS WOULD BE ORDERED AND THE LINE WOULD BE CHANGED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20519060 ↗
• MalfunctionOct 18, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED FROM THE Y-SITE (CLEARLINK) DESPITE HAVING A GREEN ALCOHOL CAP IN PLACE. THIS OCCURRED DURING PATIENT INFUSION WITH TOTAL PARENTERAL NUTRITION (TPN). THE LINE WAS REPLACED TO RESOLVE THE EVENT. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20481866 ↗
• MalfunctionOct 16, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM CONTINU-FLO SOLUTION SET LEAKED FROM THE Y-SITE PORT (CLEARLINK). THE SET WAS LEAKING DESPITE A NON-BAXTER GREEN ALCOHOL CAP BEING IN PLACE. THIS OCCURRED DURING PATIENT USE. TO RESOLVE THE EVENT, NEW FLUIDS WERE GIVEN AND THE TUBING WAS CHANGED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20463097 ↗
• MalfunctionOct 4, 2024Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET HAD A CRACK AT THE Y-SITE (CLEARLINK) RESULTING IN LEAKAGE OF TOTAL PARENTERAL NUTRITION (TPN). THIS WAS OBSERVED DURING PATIENT USE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20371862 ↗
• MalfunctionOct 4, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET LEAKED AT THE Y-SITE PORT DESPITE THE GREEN ALCOHOL CAPS BEING IN PLACE. THIS WAS NOTICED DURING USE. THE DEVICE CONTAINED TOTAL PARENTERAL NUTRITION. THE LINE WAS CHANGED TO RESOLVE THE ISSUE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20369514 ↗
• MalfunctionSep 16, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED THAT A CLEARLINK SYSTEM, NON-DEHP CONTINU-FLO SOLUTION SET WAS LEAKING FROM THE Y-SITE. THIS ISSUE WAS FURTHER DESCRIBED AS THE TUBING WAS LEAKING AT THE Y-SITE OF THE LIPID TUBING DESPITE THE GREEN ALCOHOL CAP BEING IN PLACE. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20231534 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K180739, K961225. One submission often covers many models, so check the product and lot details in each record.

• Z-0201-2026 · Aug 29, 2025 · Open, Classified
  CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 meters). Non-DEHP, Product Code 2R8519
• Z-0202-2026 · Aug 29, 2025 · Open, Classified
  CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 120-inch (3.0 meters), Non-DEHP, Product Code 2R8537
• Z-0203-2026 · Aug 29, 2025 · Open, Classified
  CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-i
• Z-1009-2025 · Dec 20, 2024 · Open, Classified
  Baxter Solution Set with Duo-Vent Spike, REF 2R8404
• Z-1010-2025 · Dec 20, 2024 · Open, Classified
  Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538
• Z-1291-2024 · Feb 8, 2024 · Open, Classified
  CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
• Z-0794-2020 · Dec 12, 2019 · Open, Classified
  ONE-LINK Needle-free IV Connector, Product Codes: 7N8300, 7N8301, 7N8310, 7N8330K, 7N8332K, 7N8334K, 7N8370K, 7N8371, 7N8375K, 7N8376K, 7N8377, 7N8378, 7N8390, 7N8391, 7N8399 - Pro
• Z-0793-2020 · Dec 12, 2019 · Open, Classified
  Clearlink System Continu-Flo Administration Sets, Product Codes: 2C8519, 2C8537, and 2C8541 - Product Usage:For the administration of fluids from a container into the patients vas
• Z-0475-2012 · Dec 6, 2011 · Terminated
  Baxter Interlink System Extension Set, 13" (32 cm), Check Valve, Injection Site, Male Luer Lock Adapter; an Rx sterile, nonpyrogenic fluid pathway for the administration of sterile
• Z-2920-2011 · Jul 21, 2011 · Terminated
  Baxter Solution Set with Duo-Vent Spike; 109" (2.8 m), Male Luer Lock Adapter 10 drops/mL. Baxter Healthcare Corporation. A sterile, single use, nonpyrogenic fluid pathway for use
• Z-0653-06 · Dec 15, 2005 · Terminated
  Baxter Interlink System Continu-Flo Solution Set with Standard Bore 4-Way Stopcock Manifold Extension Set and Minivolume Extension Set, product code 3C0078; An Rx sterile, nonpyrog
• Z-0845-05 · Feb 28, 2005 · Terminated
  Baxter ClearLink Intravenous (IV) Solution Sets and Extension Sets that have a ClearLink luer activated valve for IV access, which allows the administration of medications/solutio
• Z-1152-03 · Jul 16, 2003 · Terminated
  Interlink System Continu-Flo Solution Set with Microbore Tubing, 60 drops/mL, 128'', 3 injection sites, Male Luer Lock Adapter, catalog 2C6521; Baxter Healthcare Corporation, Deerf