ICU Medical CL-13-5Recalls & reported problems
Icu Medical, Inc. · 30" (76 cm) 20 Drop Admin Set w/Integrated ChemoLock™ Port Drip Chamber, ChemoLock™; 5 Units · 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 00887709097452), received between Feb 13, 2026 and Feb 13, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
60 other recalls cover devices cleared under the same FDA submission (K131549); 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
- Detachment of Device or Device Component1
- Fluid/Blood Leak1
- Particulates1
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.
MalfunctionFeb 13, 2026Fluid/Blood Leak; Particulates; Detachment of Device or Device Component
AN EVENT INVOLVED A A CHEMOLOCK BAG SPIKE WITH ADDITIVE PORT, 5 UNITS WHERE THE CUSTOMER REPORTED THAT THE PRODUCT HAD RANDOM SHOWING OF WHAT LOOKS LIKE UV GLUE IN TUBING, AND DETACHMENT OF THE PORT ON THE 13 WHICH LED TO A LEAK OF CYCLOPHOSPHAMIDE THERE WAS PATIENT INVOLVEMENT AND NO HARM/ADVERSE EVENT REPORTED. THIS OCCURRED 2 TIMES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24335350 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K131549. One submission often covers many models, so check the product and lot details in each record.
- Z-3159-2026 · May 12, 2026 · Open, ClassifiedOncology sets with drip chambers
- Z-3161-2026 · May 12, 2026 · Open, ClassifiedIV Sets with drip chambers
- Z-2210-2026 · Mar 24, 2026 · Open, ClassifiedOncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL
- Z-0351-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical 21" Ext Set w/ChemoLock Port, Clamp, Graduated Connector REF: CL3360
- Z-0345-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Vented Vial Spike, 13mm REF: CL-72
- Z-0349-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock 13mm Closed Vial Spike REF: CL-82
- Z-0348-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Closed Vial Spike w/Skirt, 5 Units REF: CL-80S-5
- Z-0344-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Vented Vial Spike, 20mm REF: CL-70S
- Z-0362-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Oncology Kit w/2 ChemoLock", 13mm Closed Vial Spike w/ChemoLock" Port, ChemoLock" Bag Spike, Ext Set w/ChemoLock" Port, Clamp, Graduated Adapter REF: CL4188
- Z-0331-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Clave Bag Spike w/ChemoLock Port REF: CL2150
- Z-0363-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemosafeLock Bag Spike REF: KL-BS001U3
- Z-0352-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Graduated Connector w/ChemoLock Port REF: CL3900
- Z-0365-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemosafeLock Vial Adapter REFs: KL-VA001U3 KL-VA002U3 KL-VA131U3 KL-VA201U3 KL-VA202U3 KL-VA321U3
- Z-0329-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Chemo Lock Universal Vented Vial Spike REF: CL-70-10
- Z-0328-2026 · Sep 8, 2025 · Open, ClassifiedChemoLock Bag Spike, 01 units REF: CL-10-10
…and 45 more.
Other Closed antineoplastic and hazardous drug reconstitution and transfer system devices
- BD PhaSeal 515003BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall183 reports
- BD PhaSeal 515056BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall159 reports
- BD PhaSeal Optima 515070BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall154 reports
- Alaris 10012241-0500BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall138 reports
- BD PhaSeal 515005BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall128 reports
- ICU Medical CL3011Icu Medical, Inc. · Closed antineoplastic and hazardous drug reconstitution and transfer system3 recalls26 reports
- BD PhaSeal Optima 515052BD Switzerland Sàrl · Closed antineoplastic and hazardous drug reconstitution and transfer system1 recall114 reports
- ICU Medical CL3511Icu Medical, Inc. · Closed antineoplastic and hazardous drug reconstitution and transfer system3 recalls6 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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