ICU Medical B30183Recalls & reported problems

Summary

The FDA's MAUDE database contains 30 adverse event reports that list this exact device (DI 00887709055445), received between Aug 23, 2023 and Mar 20, 2024 — classified as 30 malfunctions.

The most frequently reported specific device problem is “Air/Gas in Device” (30 reports).

188 other recalls cover devices cleared under the same FDA submission (K964435); 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 30 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 20, 2024Air/Gas in Device; Air/Gas in Device

  IT WAS REPORTED THAT A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER ALLOWED AIR TO ENTER THE TUBING, TRAPPING FLUID ABOVE IN THE BAG AND DRIP CHAMBER DURING PATIENT USE. THEN AIR IN THE TUBING DOWN TO THE FILTER AND THERE IS FLUID BELOW THE FILTER. THEY ARE UNABLE TO BACK PRIME TO CLEAR THE LINE OF AIR AND RUN THE MEDICINE. THE DEVICE IS CONTAMINATED WITH CHEMOTHERAPY. THERE WAS A PATIENT INVOLVED, NO PATIENT HARM AND THERE WAS A DELAY IN THERAPY AS THE DRUG HAD TO BE REMADE TO COMPLETE THE THERAPY. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18947294 ↗
• MalfunctionMar 19, 2024Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE THE CUSTOMER REPORTED THAT AIR ENTERED THE TUBING, TRAPPING FLUID ABOVE IN THE BAG AND DRIP CHAMBER THEN AIR IN THE TUBING DOWN TO THE FILTER AND THERE¿S FLUID BELOW THE FILTER. THE CUSTOMER REPORTED THAT THEY ARE UNABLE TO BACK PRIME AND CLEAR THE LINE OF AIR AND RUN THE MEDICINE. THE CUSTOMER REPORTED THAT THERE WAS PATIENT INVOLVEMENT BUT NO PATIENT HARM AND THAT THERE WAS DELAY IN THERAPY AS THEY NEEDED TO REWORK AND REPRIME TO GET THE ENTIRE DOSE TO RUN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18937592 ↗
• MalfunctionMar 18, 2024Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE IT WAS REPORTED THAT AIR ENTERED THE TUBING, TRAPPING FLUID ABOVE IN THE BAG AND DRIP CHAMBER. THERE WAS ALSO AIR IN THE TUBING DOWN TO THE FILTER AND THERE WAS FLUID BELOW THE FILTER. IT WAS STATED THEY WERE UNABLE TO BACK PRIME AND CLEAR THE LINE OF AIR TO RUN THE MEDICINE. THERE WAS PATIENT INVOLVED AND A DELAY IN THERAPY DUE TO HAVING TO REPRIME. SOME MEDICATION WAS NOT ABLE TO BE ADMINISTERED DUE TO ISSUES WITH THE TUBING. NO REPORT OF HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18920769 ↗
• MalfunctionMar 12, 2024Air/Gas in Device; Air/Gas in Device

  IT WAS REPORTED THAT A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER ALLOWED AIR IN THE LINE DURING PATIENT USE. IT WAS REPORTED THAT THEY ARE HAVING SIGNIFICANT ISSUES WITH FILTERED SECONDARY TUBING FOR THEIR CHEMOTHERAPY ADMINISTRATION. IN ADDITION, THEY HAVE HAD AN AIR PROXIMAL, FILTER ON THE SET SHOWN WITH FLUID IN THE BAG, DRIP CHAMBER, AND PROXIMAL TUBING. AIR BUBBLES WERE SEEN MOVING PROXIMAL IN THE LINE AND THINKS THE AIR IS BEING SUCKED INTO THE FILTER. THE SET WAS USED IN ONCOLOGY INFUSION WITH HAZARDOUS DRUGS. THE CLOSED SYSTEM DRUG-TRANSFER DEVICE (CSTD) USED WAS EQUASHIELD. THE SET WAS PRIMED ACCORDING TO INSTRUCTIONS AND THE DRIP CHAMBER WAS FILLED BEFORE THE BUBBLES WERE NOTED. THE TUBING WAS BACK PRIMED AND ABLE TO FINISH THE MAJORITY OF THE INFUSION WITHOUT REPLACEMENT. THERE WAS A PATIENT INVOLVED, NO PATIENT HARM/INJURY WAS REPORTED AND THERE WAS A DELAY IN INFUSION TO CLEAR AIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18891827 ↗
• MalfunctionSep 13, 2023Air/Gas in Device; Air/Gas in Device

  IT WAS REPORTED THAT A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER GENERATED AIR IN THE FILTER MID-WAY THROUGH INFUSION. THE MEDICATION INVOLVED WAS VECTIBIX AT 216 ML/HR AND THE EVENT WAS NOTICED AT 1250. THERE WAS PATIENT INVOLVEMENT AND NO HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17736960 ↗
• MalfunctionSep 12, 2023Air/Gas in Device; Air/Gas in Device

  THE INCIDENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER. IT WAS STATED IN THE REPORT THAT AIR IN LINE TOWARDS END OF INFUSION. THE MEDICATION INVOLVED IS ENHURTI, WITH INFUSION RATE OF 220 ML/HR. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17732372 ↗
• MalfunctionSep 11, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER. IT WAS REPROTED THAT AIR WAS NOTED IN FILTER MID WAY. THE EVENT OCCURRED ON (B)(6) 2023, AND THE MEDICATION INVOLVED IS ENHURTU, WITH INFUSION RATE OF 118 ML/HR. THERE WAS PATIENT INVOLVEMENT AND NO HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17726523 ↗
• MalfunctionSep 11, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH WAS REPORTED TO HAVE AIR IN THE LINE OBSERVED TOWARD THE END OF TAXOL INFUSION AT THE RATE OF 275 ML/HR. THERE WAS PATIENT INVOLVEMENT; HARM WAS NOT REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17725207 ↗
• MalfunctionSep 11, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH HAD AIR IN LINE OBSERVED TOWARDS END OF TAXOL INFUSION AT THE RATE OF 182ML/HR. THERE WAS PATIENT INVOLVEMENT; HARM WAS NOT REPORTED AS CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17724158 ↗
• MalfunctionSep 11, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH WAS REPORTED TO HAVE AIR IN LINE WHICH WAS OBSERVED TOWARDS END OF TAXOL INFUSION AT A RATE OF 183 ML/HR. THERE WAS PATIENT INVOLVEMENT; HARM WAS NOT REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17723167 ↗
• MalfunctionSep 11, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE AN AIR IN LINE TOWARDS THE END OF DURVALUMAB INFUSION WAS REPORTED AT 12:59. THE INFUSION RATE WAS 280 ML/HR. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17722844 ↗
• MalfunctionSep 11, 2023Fluid/Blood Leak; Air/Gas in Device; Fluid/Blood Leak; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE AN AIR IN LINE TOWARDS END OF INFUSION WAS REPORTED. THE EVENT OCCURRED AT 1100 INVOLVING ETOPOSIDE. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17719345 ↗
• MalfunctionSep 8, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH WAS REPORTED TO HAVE AIR OBSERVED IN THE LINE TOWARDS END OF INFUSION OF ETOPOSIDE; INFUSION RATE 508ML/HR. THERE WAS PATIENT INVOLVEMENT; NO HARM WAS REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17714443 ↗
• MalfunctionSep 8, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE IT WAS REPORTED THERE WAS AIR IN LINE TOWARDS END OF INFUSION, HAD TO BACK PRIME MULTIPLE TIMES. THE EVENT OCCURRED DURING INFUSION OF CETUXIMAB WITH INFUSION RATE OF 175 ML/HR. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17710666 ↗
• MalfunctionSep 6, 2023Air/Gas in Device; Air/Gas in Device

  THE REPORTED COMPLAINT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER THAT WAS REPORTED TO HAVE AIR IN THE LINE, TOWARDS THE END OF A PATIENT'S TAXOL INFUSION (INFUSION RATE 177ML/HR). THERE WAS NO REPORT OF HUMAN HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17690570 ↗
• MalfunctionSep 5, 2023Air/Gas in Device; Air/Gas in Device

  THE INCIDENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER. IT WAS REPORTED THAT THERE WAS AIR IN THE LINE TOWARD THE END OF THE INFUSION. THE MEDICATION INVOLVED IS RAMUCIRUMAB WITH INFUSION RATE OF 297 ML/HR. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17683925 ↗
• MalfunctionSep 5, 2023Air/Gas in Device; Air/Gas in Device

  THE REPORTED COMPLAINT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER. TOWARDS THE END OF THE PATIENT'S INFUSION, AIR IN LINE WAS REPORTED . AS A RESULT, BACK-PRIMING WAS REQUIRED FOUR TIMES IN ORDER TO COMPLETE THE TAXOL DELIVERY (INFUSION RATE OF 188 ML/HR). THERE WAS NO HUMAN HARM REPORTED AS A RESULT OF THIS COMPLAINT/EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17683118 ↗
• MalfunctionSep 1, 2023Air/Gas in Device; Air/Gas in Device

  IT WAS REPORTED THAT A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WAS FOUND TO HAVE AIR IN THE FILTER TOWARDS THE END OF INFUSION AND THE MEDICATION INVOLVED IS TAXOL 275ML/HR. THERE WAS PATIENT INVOLVEMENT BUT NO HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17671985 ↗
• MalfunctionSep 1, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER. IT WAS REPORTED THAT AIR IN LINE TOWARDS END OF INFUSION, SECOND DAY PATIENT HAS HAD THIS HAPPENED (D2 CHEMO). MEDICATION INFUSING WAS ETOPOSIDE 508 ML/HOUR. NO PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17669464 ↗
• MalfunctionAug 31, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT OCCURRED ON AN UNKNOWN DATE INVOLVING A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE THE PATIENT REPORTED THAT AIR GETS BACK UP INTO THE FILTER CAUSING HIS CHEMO TREATMENT NOT TO COMPLETE. THERE WAS A PATIENT INVOLVED AND NO HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17663044 ↗
• MalfunctionAug 31, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH THE CUSTOMER REPORTED THAT THEY OBSERVED AIR IN FILTER AT THE BEGINNING AND END OF THE INFUSION OF TAXOL 177ML/HR. THERE WAS PATIENT INVOLVEMENT, BUT NO HARM WAS REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17662311 ↗
• MalfunctionAug 31, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT OCCURRED ON AN UNKNOWN DATE INVOLVING A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHERE IT WAS REPORTED THAT AIR WAS NOTED FROM THE FILTER AREA ALL THE WAY TO THE PUMP WITH RESIDUAL MEDICATION IN TUBING LEADING FROM FILTER TO THE BOTTOM OF THE BAG. BACK PRIMING PERFORMED THREE TIMES TO ATTEMPT TO REMOVE AIR, BUT AIR DOES NOT GO PASS THE FILTER AREA. THE PATIENT REFUSED TO WAIT FOR THE SECONDARY LINE TO BE SENT BACK TO PHARMACY FOR PRIMING. THE PATIENT REQUESTED TO BE DISCHARGED. THE MEDICATION INVOLVED WAS ETOPOSIDE 506ML/HR. THERE WAS PATIENT INVOLVEMENT BUT NO REPORT OF ADVERSE REACTION OR NEED FOR MEDICAL INTERVENTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17662200 ↗
• MalfunctionAug 31, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER WHICH WAS REPORTED TO HAVE AIR IN THE FILTER NOTICED DURING PATIENT USE. THE INCIDENT OCCURRED AT 11:30 AND 11:45 ON SAME PATIENT. THE MEDICATION INVOLVED WAS CETUXIMAB 268ML/HR. THERE WAS PATIENT INVOLVEMENT, HOWEVER, HARM WAS NOT REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17660949 ↗
• MalfunctionAug 29, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER, WHERE IT WAS REPORTED THAT THERE WAS AIR IN LINE, AND THE MEDICATION INVOLVED IS TAXOL 182ML/HR. THERE WAS UNKNOWN PATIENT INVOLVEMENT AND UNKNOWN ADVERSE REACTION OR NEED FOR MEDICAL INTERVENTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17646025 ↗
• MalfunctionAug 29, 2023Air/Gas in Device; Air/Gas in Device

  THE EVENT INVOLVED A 32" (81 CM) APPX 6.3 ML, 15 DROP ADMIN SET W/0.2 MICRON FILTER, ROTATING LUER W/FILTER CAP, BAG HANGER, WHERE IT WAS REPORTED THAT THERE WAS AN OCCLUSION AND AIR IN LINE. THE MEDICATION INVOLVED IS ETOPOSIDE 505ML/HR. THERE WAS UNKNOWN PATIENT INVOLVEMENT AND UNKNOWN ADVERSE REACTION OR NEED FOR MEDICAL INTERVENTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17645511 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K964435. One submission often covers many models, so check the product and lot details in each record.

• Z-3157-2026 · May 12, 2026 · Open, Classified
  IV Non-Dedicated Gravity Administration Sets with drip chambers
• Z-3163-2026 · May 12, 2026 · Open, Classified
  IV Sets with drip chambers
• Z-0154-2026 · Oct 2, 2025 · Open, Classified
  IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B
• Z-1721-2022 · Aug 1, 2022 · Open, Classified
  6.5" (17 cm) Appx 0.84 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, 2 Check Valves, Luer Lock;
• Z-0957-2021 · Dec 2, 2020 · Terminated
  7 IN (18cm) APPX 0.43ml, SMALLBORE SET, MicroCLAVE, FILTER SetSource - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which pro
• Z-0956-2021 · Dec 2, 2020 · Terminated
  60" (152 cm) Appx 1.9 ml, Smallbore Ext Set w/MicroClave Clear, 1.2 Micron Filter, 2 Clamps, Luer Lock REF MC330174 - Product Usage: The intravascular administration set is a singl
• Z-0955-2021 · Dec 2, 2020 · Terminated
  60 IN (152cm) APPX 1.5 ml, PUR YELLOW SMALLBORE SET, FILTER REF B2209 - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which pr
• Z-0958-2021 · Dec 2, 2020 · Terminated
  154 cm (61 IN) APPX 1.5ml, PUR YELLOW EXT, 1.2 MICRON FILTER - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides ac
• Z-0258-2021 · Jul 6, 2020 · Terminated
  112" (284 cm) 60 Drop 150ml Burette Set (Clave, Shut-Off) w/2 MicroClave, Remv 3 Gang 4-Way Clave Stopcock, Check Valve, Rotating Luer, 1 Ext. 1 unit per pouch, 25 pouches per case
• Z-0262-2021 · Jul 6, 2020 · Terminated
  8 IN (20CM) APPX 1.3ml, EXT SET w/3-Port NanoClave Manifold, Check Valve.1 unit per pouch, 50 pouches per case. UDI:(01)10887709085814(17)250101(30)50(10)4605676. CLAVE Neutron i
• Z-0240-2021 · Jul 6, 2020 · Terminated
  11 IN(28cm)APPX 0.97ml,SMALLBORE SET,NanoClave,6-PORT NanoClave MANIFOLD,BCV.1 unit per pouch, 50 pouches per case. UDI:(01)10887709088354(17)250101(30)50(10)4557643. The Intrava
• Z-0256-2021 · Jul 6, 2020 · Terminated
  149 IN (378cm) APPX 19.1 ml, 15 DROP SET, 3 Clave, REMV 3 GANG 4-WAY Clave STOPCOCK 2 EXT. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709074696(17)250101(30)25(10)4711277;
• Z-0191-2021 · Jul 6, 2020 · Terminated
  5" (13 cm) Appx 0.39 ml, Smallbore Bifuse Ext Set w/NanoClave T-Connector, 2 Clamps, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709053028(17)250101
• Z-0209-2021 · Jul 6, 2020 · Terminated
  9.5" (24 cm) 0.53 ml, Smallbore Bifuse Ext Set w/NanoClave, 3 Clamps, Rotating Luer;1 unit per pouch, 50 multivac pouches per case. UDI: (01)10887709090238(17)250101(30)50(10)45729
• Z-0230-2021 · Jul 6, 2020 · Terminated
  114" (290 cm) 60 Drop 150ml Burette Set (Clave, Shut Off, Filter) w/4 Clave Remv 3-Port NanoClave Manifold, 2 Check Valves, Rotating Luer, 2 Exts. 1 unit per pouch, 25 pouches per

…and 173 more.