ICU Medical B6013Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887709011038), received between Sep 18, 2024 and Jan 8, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 8, 2025Fluid/Blood Leak; Fluid/Blood Leak

  THE EVENT STATED THAT THE ANTI-SIPHON VALVE ON LIPIDS WAS FOUND TO BE LEAKING AROUND 4AM AFTER GIVING MORPHINE INFUSION VIA MED LINE. LIPIDS WERE REMOVED AND FLUSH PLACED ON ANTI-SIPHON AND LIQUID SHOT OUT WHEN IT WAS FLUSHED. ENTIRE TPN/IL SET UP HAD TO BE CHANGED DUE TO LEAK. THE EVENT OCCURRED IN THE HOSPITAL DURING USE ON A PATIENT. THERE WAS PATIENT INVOLVEMENT AND NO ADVERSE EVENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21104213 ↗
• MalfunctionSep 18, 2024Fluid/Blood Leak; Fluid/Blood Leak

  A COMPLAINT ON AN UNKNOWN DATE IN JUNE INVOLVING AN ANTI-SIPHON VALVE EXPERIENCED LEAKAGE. IT WAS REPORTED THAT THE ANTI-SIPHON VALVE WAS LEAKING ONTO THE BED. EDUCATOR WAS BROUGHT IN TO ASSESS. ANTI-SIPHON VALVE WAS REMOVED. VALVE ITSELF LOOKED INTACT BUT WAS LEAKING. THERE WAS A PATIENT INVOLVEMENT AND NO ADVERSE EVENT. UPDATE 1: THE REPORTER ALSO STATED THAT "I HAPPENED TO BE CALLED INTO A ROOM WHEN THE BEDSIDE NURSE HAD NOTED THAT AN ANTI-SIPHON VALVE ON HER LIPID INFUSION WAS LEAKING. THE ANTI-SIPHON VALVE WAS REMOVED, AND I PERSONALLY ATTACHED A SALINE FLUSH TO CHECK AND SEE IF IT WAS STILL LEAKING AND IT WAS. I NOTICED IT WAS LEAKING WHERE IT WAS CONNECTED TO MY SALINE SYRINGE SO I REMOVED IT AND REPLACED IT AGAIN ALSO ENSURING IT WAS TIGHT SO THAT I COULD BE POSITIVE IT WASN¿T USER ERROR. IT CONTINUED TO LEAK. THE NURSE STATED THAT SHE HAD NOT NOTICED IT LEAKING PRIOR TO THIS. I THEN REMOVED A NEW ANTI-SIPHON VALVE FROM A PACKAGE AND CHECKED THAT WITH THE SALINE SYRINGE AND THERE WAS NO LEAKING."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20252957 ↗

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-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-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-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-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-0245-2021 · Jul 6, 2020 · Terminated
  126 IN (320cm) APPX 23.5ml, 10 Drop Set 3 Clave, Remv Clave Stopcock, 2 Ext.1 unit per pouch, 25 pouches per case. UDI:(01)10887709062365(17)250201(30)25(10)4630752. The Intrav
• Z-0187-2021 · Jul 6, 2020 · Terminated
  7" (18cm) Appx 0.31 ml, Smallbore Ext Set w/Remv MicroClave Clear, NanoClave T-Connector, Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)108877090510
• Z-0224-2021 · Jul 6, 2020 · Terminated
  3-Port NanoClave Manifold w/Check Valve, Rotating Luer. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709087153(17)250101(30)50(10)4556715; (01)10887709087153(17)250101(30)50
• Z-0186-2021 · Jul 6, 2020 · Terminated
  7" (18 cm) Appx 0.29 ml, Smallbore Ext Set w/MicroClave Clear, NanoClave, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709051048(17)250101(30)
• Z-0237-2021 · Jul 6, 2020 · Terminated
  20 IN(51cm) APPX 2.5ml, Ext w/6-Port NanoClave Manifold, Check Valve.1 unit per pouch, 50 pouches per case. UDI:(01)10887709069203(17)250201(30)50(10)4742130; (01)10887709069203(1
• Z-0249-2021 · Jul 6, 2020 · Terminated
  6 IN (15 cm) Ext Set, MicroClave Clear, T-Connector, RLL, Approx PV: 0.86 mL.1 unit per pouch, 50 pouches per case. UDI:(01)10887709079877(17)250101(30)50(10)4584753;(01)108877090
• Z-0219-2021 · Jul 6, 2020 · Terminated
  113" (287 cm) Appx 14.7 ml, 10 Drop Admin Set w/MicroClave" Clear, Remv 4-Way NanoClave" Stopcock, Remv 2-Gang 4-Way NanoClave" Stopcocks, Spin Luer w/ Filter Cap, 2 Ext.1 unit per

…and 173 more.