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ICU Medical B6015Recalls & reported problems

Icu Medical, Inc. · Back Check Valve · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887709011045), received between Nov 8, 2024 and Nov 8, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 1 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Fluid/Blood Leak1
  • No Flow1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 8, 2024Fluid/Blood Leak; No Flow; Fluid/Blood Leak; No Flow

    THE EVENT INVOLVED A BACK CHECK VALVE WHERE IT WAS REPORTED THAT THE BACK VALVE DOES NOT WORK- IT HAD MANY ISSUES WITH THE MEDICATION BACKING UP AND PATIENT NOT GETTING THE ADEQUATE MEDS. THERE WAS PATIENT INVOLVEMENT BUT NO HARM. HOWEVER, THE MEDICATIONS BACK UP AND FLOW ONTO THE BED IN SEVERAL OCCASIONS. THEY DID NOT DO WHAT THEY ARE SUPPOSED TO DO. THIS HAS OCCURRED ON SEVERAL DAYS IN OCTOBER AND SEPTEMBER AS REPORTED BY MULTIPLE CRNAS. IT OCCURRED DURING THE CASES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20642257 ↗

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-3163-2026 · May 12, 2026 · Open, Classified
    IV Sets with drip chambers
  • Z-3157-2026 · May 12, 2026 · Open, Classified
    IV Non-Dedicated Gravity Administration 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-0222-2021 · Jul 6, 2020 · Terminated
    123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave; UDI:(01)10887709085432(17)241201(30)25(10)4536733;(01)10887709085432(17)250101(30)25(10)4573641. The In
  • Z-0255-2021 · Jul 6, 2020 · Terminated
    148 IN (376cm) APPX 18.8 ml, 15 DROP SET, 2 CLAVE, Remv 3 Gang Clave Stopcock.1 unit per pouch, 25 pouches per case. UDI:(01)10887709071558(17)250101(30)25(10)4603841. The Intrav
  • 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
  • Z-0226-2021 · Jul 6, 2020 · Terminated
    112 IN(284cm) APPX 14.6ml, 15 Drop Set 3 MicroClave, 3-Port NanoClave Manifold, BCV.1 unit per pouch, 25 pouches per case. UDI:(01)10887709088518(17)241101(30)25(10)4475764 (01)108
  • Z-0196-2021 · Jul 6, 2020 · Terminated
    7.5" (19 cm) Appx 0.59 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear (Yellow, Green, Purple Rings), NanoClave T-Connector, 4 Clamps, Rotating Luer. UDI:(01)10887709067049(17)2
  • Z-0188-2021 · Jul 6, 2020 · Terminated
    10" (25 cm) Appx 2.8 ml, Trifuse Ext Set w/3 MicroClave Clear, Tri-Connector, NanoClave T-Connector, 4 Clamps (Red, White, Blue), Rotating Luer;1 unit per pouch, 50 multivac pouche
  • Z-0208-2021 · Jul 6, 2020 · Terminated
    12" (30 cm) Appx 0.67 ml, Smallbore Ext Set w/NanoClave, 0.2 Micron Filter, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709049496(17)250101(3

…and 173 more.

Other Stopcock, i.V. Set devices

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Sources and updates

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