ICU Medical CL-12Recalls & reported problems
Icu Medical, Inc. · ChemoLock™ Bag Spike with Additive Port, Dry Spike · 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
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00887709056978), received between Dec 16, 2019 and Nov 14, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (3 reports).
1 FDA recall record name this device's identifier, 1 still open.
59 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
Recalls naming this device
- Jun 27, 2022Class IIOpen, Classified
Ports have a potential for unintended disconnection, inability to connect to or fully engage with injectors, due to a variation in the spring inside the Port, which may cause delay of therapy and exposure to caustic substances. Ports available as standalone connectors, or utilized as access points on vial adaptors, bag spikes, and administration sets.
Z-1681-2022 · Root cause: Component design/selection · Recall details · FDA record ↗
Most reported problems
Device problems
- Fluid/Blood Leak3
- Disconnection1
- Unintended Movement1
Patient problems
- Chemical Exposure1
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 14, 2025Fluid/Blood Leak; Fluid/Blood Leak
A COMPLAINT WAS RECEIVED WITH REGARDS TO A CHEMO LOCK BAG SPIKE WITH ADDITIVE PORT, DRY SPIKE IN WHICH IT WAS REPORTED THAT THERE WAS A CHEMO SPILL ON CHEMO LOCK BAG SPIKE FROM THE IV SOLUTION SODIUM CHLORIDE BAG. THE PATIENT INVOLVEMENT NOT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23560248 ↗MalfunctionNov 13, 2025Disconnection; Fluid/Blood Leak; Disconnection; Fluid/Blood Leak
A COMPLAINT WAS RECEIVED WITH REGARDS TO A CHEMOLOCK BAG SPIKE WITH ADDITIVE PORT, DRY SPIKE IN WHICH IT WAS REPORTED THAT THERE WAS A CHEMO SPILL. THE EVENT OCCURRED WHEN THE RN ATTEMPTED TO HANG THE BAG. THE RN SPILLED CHEMO AGENT OVER HER ARM WHILE WEARING PERSONAL PROTECTIVE EQUIPMENT (PPE). THERE WAS NO PATIENT HARM.
Patient problems: Chemical Exposure
MAUDE report 23543361 ↗MalfunctionDec 16, 2019Fluid/Blood Leak; Unintended Movement; Fluid/Blood Leak; Unintended Movement
AN UPDATE WAS RECEIVED FROM THE CUSTOMER ON (B)(6) 2020 STATING THAT THE BAG THAT WAS SENT TO THE FLOOR AND CAUSED A SPILL IN THE PATIENT'S ROOM WAS A D5W 250ML.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9475867 ↗
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-3161-2026 · May 12, 2026 · Open, ClassifiedIV Sets with drip chambers
- Z-3159-2026 · May 12, 2026 · Open, ClassifiedOncology 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-0346-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Closed Vial Spike REF: CL-80
- Z-0331-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Clave Bag Spike w/ChemoLock Port REF: CL2150
- Z-0354-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Vented Vial Spike, 20mm, 20 Units REF: 011-CL-70S-20
- Z-0359-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical 31" (79 cm) Appx 3.4 ml, Admin Set w/20 Drop Integrated ChemoLock Drip Chamber, Spiros", Purple Cap, Hanger REF: CL3951
- Z-0345-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Vented Vial Spike, 13mm REF: CL-72
- Z-0363-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemosafeLock Bag Spike REF: KL-BS001U3
- Z-0339-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical 60" (152 cm) Appx 1.2 ml, Ext Set, Smallbore w/ChemoLock Port, Clamp, Spiros w/Red Cap REF: CL4173
- Z-0360-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical 7.5" (19 cm) Appx 1.5 ml, Ext Set w/ChemoLock" Port, Clamp, Graduated Adapter REF: CL3967
- Z-0356-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical Syringe Transfer Set w/MicroClave, ChemoLock Port REF: CL-34
- 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-0358-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical 8" (20 cm) Ext Set w/MicroClave Clear, ChemoLock Port, Y-Connector, Rotating Luer, REF: CL-3950
- Z-0347-2026 · Sep 8, 2025 · Open, ClassifiedICU Medical ChemoLock Vial Spike, 20mm REF: CL-80S
…and 44 more.
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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 · each recall links to the FDA recall notice
- 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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