ICU Medical Z3239Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887709030473), received between Nov 6, 2023 and Nov 8, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “No Flow” (2 reports).

1 FDA recall record name this device's identifier, 1 still open.

187 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.

Recalls naming this device

1. May 12, 2026Class IIOpen, Classified

   Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

   Z-3163-2026 · Root cause: Process control · Recall details · FDA record ↗

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.

• MalfunctionNov 8, 2023No Flow; No Flow

  THE EVENT INVOLVED A 126" 10 DROP PRIMARY SET W/3 MICROCLAVE¿, 2 GANG 4-WAY STOPCOCKS, ROTATING LUER, 1 EXT. THE CUSTOMER INITIALLY REPORTED THAT THE TUBING WOULD NOT FLOW, THE INTRAVENOUS (IV) PATIENT BLOOD RETURNED; THE IV TUBING WAS REPLACED. ADDITIONAL INFORMATION BECAME AVAILABLE VIA A MEDSUN MEDWATCH MANDATORY REPORT UF/IMPORTER REPORT # (B)(4). WHICH STATED: " IN PRE-OPERATION, ANESTHESIA TUBING WAS NOTED TO NOT BE FLOWING. ANESTHESIA TUBING WOULD NOT FLOW. PERIPHERAL INTRAVENOUS (PIV) WAS PATENT WITH POSITIVE BLOOD RETURN. IV TUBING REPLACED AND IVF FLOWING FREELY. NO REPORTED PATIENT HARM AND ONLY IVF MEDICATION NOTED TO BE RUNNING, NOT ANESTHETIC MEDICATION." THE DATE OF THE EVENT SUBMITTED ON THE MEDWATCH WAS (B)(6) 2023. 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 18092098 ↗
• MalfunctionNov 6, 2023No Flow; No Flow

  THE INCIDENT INVOLVED A 126" 10 DROP PRIMARY SET W/3 MICROCLAVE¿, 2 GANG 4-WAY STOPCOCKS, ROTATING LUER, 1 EXT. A MEDSUN MEDWATCH MANDATORY REPORT UF/IMPORTER REPORT # (B)(4) WAS RECEIVED BY THE MANUFACTURER. PER THE REPORT, NURSING NOTED THAT THE ANESTHESIA TUBING WOULD NOT ALLOW INTRAVENOUS FLUIDS (IVF) TO FLOW. THE BOTTOM LUER-LOCK PORT WAS NOT FLUSHABLE. THE PERIPHERAL IV (PIV) ITSELF WAS PATENT. THERE WAS NO REPORTED PATIENT HARM AND ONLY IVF NOTED TO BE RUNNING, NOT ANESTHETIC MEDICATION. THE ORIGINAL INTENDED PROCEDURE WAS FOR IV TUBING TO DELIVER IVF AND ANESTHETIC ONCE PATIENT WAS IN THE OPERATING ROOM. THERE WERE NO OBSERVED DAMAGES OR ANOMALIES WITH THE SET AND/OR THE MATING /ACCESS DEVICES. THERE WAS PATIENT INVOLVEMENT AND NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18074220 ↗

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-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-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-0243-2021 · Jul 6, 2020 · Terminated
  78" (198 cm) APPX 1.7ml, EXT SET, MicroClave Clear, 6-PORT NanoClave MANIFOLD, FILTER .1 unit per pouch, 50 pouches per case. UDI:(01)10887709121703(17)250201(30)50(10)4723226.
• Z-0239-2021 · Jul 6, 2020 · Terminated
  APPX 0.75 ml, 6-Port NanoClave Manifold, Check Valve. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709070551(17)241201(30)50(10)4542066; (01)10887709070551(17)241201(30)50(1
• 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-0231-2021 · Jul 6, 2020 · Terminated
  10 IN (25cm) APPX 1.5ml, Ext w/3-Port NanoClave Manifold, Check Valve. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709080796(17)241201(30)50(10)4536743; (01)1088770908
• Z-0189-2021 · Jul 6, 2020 · Terminated
  9" (23 cm) Appx 0.63 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, NanoClave, 3 Clamps, 0.2 Micron Filter, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case UDI:(0
• Z-0242-2021 · Jul 6, 2020 · Terminated
  11 IN (28cm) APPX 1.5ml EXT SET NanoClave, 6-Port NanoClave Manifold . 1 unit per pouch, 50 pouches per case. UDI:(01)10887709098937(17)241201(30)50(10)4493669;(01)10887709098937(
• 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-0247-2021 · Jul 6, 2020 · Terminated
  7 IN (18CM) APPX 0.26ml, SMALLBORE EXT SET, MicroClave, Clave T-Connector.1 unit per pouch, 50 pouches per case. UDI: (01)10887709018065(17)250101(30)50(10)4572133. The Intravasc

…and 172 more.