ICU Medical B9900-217Recalls & reported problems
Icu Medical, Inc. · 109" (277 cm) Appx 20.6 mL, 15 Drop 24 Hour Primary Set w/2 Bravo24®, Pre-Slit Port, Rotating Luer · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887709016613), received between Mar 30, 2026 and Mar 31, 2026 — 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.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 31, 2026Fluid/Blood Leak
AN EMAIL WAS RECEIVED REGARDING THE PRODUCT 218 CM 20 DROP PRIMARY SET W/2 MICROCLAVE IN WHICH IT WAS REPORTED THAT LEAKING REPORTED AT THE TOP CLAVE /YSITE CONNECTION. 6 SETS LEAKING FROM SAME BOX, BUT ONLY FROM EMERGENCY ROOM. NONE OF THE OTHER UNITS AFFECTED. IT WAS STOPPED IMMEDIATELY AND INSERVICE TRAINING DONE AND ALL OTHER UNITS CHECKED FOR ANY OTHER CONCERNS. FIRST SETS WAS REPLACED AND THEY KEEP ON MONITORING IF ANY OTHER SETS AFFECTED. THERE WAS PATIENT INVOLVEMENT AND DELAY IN THERAPY, BUT NO PATIENT HARM NOTED. THIS IS REPORT 1 OF 2 FOR THE EMERGENCY ROOM EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24740500 ↗MalfunctionMar 30, 2026Fluid/Blood Leak
AN EMAIL WAS RECEIVED REGARDING THE PRODUCT 218CM 20 DROP PRIMARY SET W/2 MICROCLAVE IN WHICH IT WAS REPORTED THAT LEAKING REPORTED AT THE TOP CLAVE /YSITE CONNECTION. 6 SETS LEAKING FROM SAME BOX, BUT ONLY FROM ER. NONE OF THE OTHER UNITS AFFECTED. THE STATUS OF THE PRODUCT AT THE TIME OF THE EVENT WAS DURING USE ON PATIENT. IT WAS STOPPED IMMEDIATELY AND INSERVICE TRAINING DONE AND ALL OTHER UNITS CHECKED FOR ANY OTHER CONCERNS. UNIT MANAGER AND STAFF REPORTED IT. FIRST SETS WAS REPLACED AND THEY KEEP ON MONITORING IF ANY OTHER SETS AFFECTED. THERE WAS PATIENT INVOLVEMENT AND DELAY IN THERAPY, BUT NO PATIENT HARM NOTED. THIS IS REPORT 2 OF 2 FOR THE OTHER 5 SETS WITH NO FURTHER INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24736451 ↗
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, ClassifiedIV Sets with drip chambers
- Z-3157-2026 · May 12, 2026 · Open, ClassifiedIV Non-Dedicated Gravity Administration Sets with drip chambers
- Z-0154-2026 · Oct 2, 2025 · Open, ClassifiedIV 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, Classified6.5" (17 cm) Appx 0.84 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, 2 Check Valves, Luer Lock;
- Z-0955-2021 · Dec 2, 2020 · Terminated60 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-0957-2021 · Dec 2, 2020 · Terminated7 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-0958-2021 · Dec 2, 2020 · Terminated154 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-0956-2021 · Dec 2, 2020 · Terminated60" (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-0224-2021 · Jul 6, 2020 · Terminated3-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-0237-2021 · Jul 6, 2020 · Terminated20 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-0227-2021 · Jul 6, 2020 · Terminated142 IN (361cm) APPX 18.8 ml, 15 DROP SET 4 MicroClave CLEAR, REMV 3-PORT NanoClave w/ BCV. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709089393(17)250101(30)25(10)4573948
- Z-0198-2021 · Jul 6, 2020 · Terminated107" (272 cm) Appx 9.1 ml, Smallbore Ext Set w/2 Check Valves, NanoClave T-Connector, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI: (01)10887709085005(
- Z-0218-2021 · Jul 6, 2020 · Terminated126" (320 cm) 16.4 ml, 15 Drop Primary Set w/2 MicroClave Clear, Remv 2 Gang 4-Way NanoClave Stopcock, Rotating Luer, 1 Ext; 1 unit per pouch, 50 multivac pouches per case. UDI:(01
- Z-0233-2021 · Jul 6, 2020 · Terminated139" (353 cm) 15 Drop Admin Set w/3 MicroClave Clear, 4-Way Stopcock, 3-Port NanoClave Manifold w/Check Valve, Spin Luer, 2 Ext. 1 unit per pouch, 25 pouches per case. UDI:(01)1088
- Z-0230-2021 · Jul 6, 2020 · Terminated114" (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.
Other Stopcock, i.V. Set devices
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- ICU Medical AC135Icu Medical, Inc. · Stopcock, i.V. Set1 recall10 reports
- IV Administration Set 490067B. Braun Medical Inc. · Stopcock, i.V. Set1 recall9 reports
- ICU Medical MC330174Icu Medical, Inc. · Stopcock, i.V. Set1 recall4 reports
- ICU Medical Z2587Icu Medical, Inc. · Stopcock, i.V. Set1 recall3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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