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ICU Medical MRSA60-84Recalls & reported problems

Icu Medical, Inc. · 84" (213 cm) 60 Drop, Vented/Non-Vented Gravity Admin Set w/Y Site, 2 MicroClave™ Clear, Rotating Luer, Approx Priming Volume: 10.8 mL · Class 2

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

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887709079502), received between Jun 14, 2024 and Jun 14, 2024 — 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.

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: 2 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 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 reports2024202520262
Last 36 months. The most recent month may be incomplete.

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 that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.

    Z-3157-2026 · Root cause: Process control · Recall details · FDA record ↗

Most reported problems

Device problems

  • No Flow2

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.

  • MalfunctionJun 14, 2024No Flow; No Flow

    IT WAS REPORTED THAT AN 84" (213 CM) 60 DROP, VENTED/NON-VENTED GRAVITY ADMIN SET W/Y SITE, 2 MICROCLAVE® CLEAR, ROTATING LUER, APPROX PRIMING VOLUME: 10.8 ML GENERATED A NO-FLOW EVENT DURING USE. IT WAS REPORTED THAT THE NURSES AND ANESTHESIOLOGIST REPORTED THAT ON WEEK (B)(6) 2024, THE NEEDLESS PORT VALVE DOESN'T OPEN UP WHEN THE MEDLINE IS SCREWED IN. THEREFORE, THE MED WILL NOT INFUSE. IT HAS HAPPENED SEVERAL TIMES NOW WITH THIS BATCH. THEY ORDERED 4 CASES AND HAVE ONLY OPENED 1 BOX SO FAR. THE ANESTHESIOLOGIST DOESN'T WANT TO USE THE SAME BRAND. THE EVENT OCCURRED DURING ACTIVE PATIENT USE (DEVICE ACTIVELY CONNECTED TO THE PATIENT). THE MEDICATIONS INVOLVED WERE PROPOFOL AND REMIFENTANIL. THE RETURNING SAMPLES ARE NEW; THE USED ONES WERE DISPOSED OF. THE SAMPLE IS AVAILABLE FOR RETURN. THERE WAS NO INJURY/DEATH.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19540771 ↗
  • MalfunctionJun 14, 2024No Flow; No Flow

    THE EVENT INVOLVED A 84" (213 CM) 60 DROP, VENTED/NON-VENTED GRAVITY ADMIN SET W/Y SITE, 2 MICROCLAVE® CLEAR, ROTATING LUER, APPROX PRIMING VOLUME: 10.8 ML WHERE IT WAS REPORTED BY THE NURSES AND ANESTHESIOLOGIST THAT THE NEEDLESS PORT VALVE DOESN'T OPEN UP WHEN THE MEDLINE IS SCREWED IN, AND MEDICATION WILL NOT INFUSE. MEDICATIONS INVOLVED WERE PROPOFOL AND REMIFENTANIL. THE EVENT OCCURRED DURING ACTIVE PATIENT USE (DEVICE ACTIVELY CONNECTED TO THE PATIENT). THERE WAS PATIENT INVOLVEMENT, HOWEVER, NO REPORT OF PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19535667 ↗

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-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-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-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-0234-2021 · Jul 6, 2020 · Terminated
    47 IN (119cm) APPX 6.7 ml, EXT, STOPCOCK, 3-Port NanoClave MANIFOLD, MicroClave Clear. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709121154(17)250101(30)25(10)4556714; (01
  • 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-0215-2021 · Jul 6, 2020 · Terminated
    29 IN (74 cm) APPX 3.9 ml, EXT SET w/ NanoClave 4-Way Stopcock; 1 unit per pouch, 50 pouches per case. UDI:(01)10840619082533(17)250101(30)50(10)4605138. The Intravascular Admi
  • 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-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-0183-2021 · Jul 6, 2020 · Terminated
    6" (15 cm) Appx 0.26 ml, Smallbore Ext Set w/Clamp, NanoClave T-Connector, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case; UDI:(01)10887709051024(17)250101(30)50(10)
  • Z-0216-2021 · Jul 6, 2020 · Terminated
    54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock ;UDI:(01)10840619082526(17)250201(30)50(10)4718579. The Intravascular Administration Set is a single use, sterile, n
  • Z-0259-2021 · Jul 6, 2020 · Terminated
    5.5" (14 cm) Appx 0.39 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, NanoClave T-Connector, 3 Clamps, Rotating Luer.1 unit per pouch, 50 multivac pouches per case. UDI: (01)1

…and 172 more.

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Sources and updates

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