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ICU Medical recallZ-0337-2026 · ICU Medical, Inc. · initiated Sep 8, 2025

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from ICU Medical, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Port weld of drug transfer device may separate or break during use and potentially result in a leak.

FDA root cause category: Under Investigation by firm

What the company is doing

On September 8, 2025, ICU Medical issued an "Urgent Medical Device" Recall notification via E-Mail. ICU Medical ask consignees to take the following actions: 1. Check all inventory locations within your institution for the affected products listed in recall notification and discontinue use. Destroy all affected products following your institution's process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal. 2. Share this notification with all potential users of the device, to ensure they are aware of this notification. If the devices are used at another location, please ensure this communication is delivered there. 3. Complete and return the attached Customer Response Form to [email protected] within 10 days of receipt to acknowledge your understanding of this notification. 4. If you have distributed affected products to your customers, please immediately forward this notice to them. Request that they complete the response form and return it to [email protected] For further inquiries, please contact ICU Medical Customer Service via email: [email protected] or call: 1-(800)-258-5361 for additional information or technical assistance. Or contact Field Service Processing via email: [email protected] for Assistance with Customer Notifications and Response Forms.

Recall details

Recall number
Z-0337-2026
Status
Open, Classified
Initiated by the company
Sep 8, 2025
Posted by the FDA
Oct 27, 2025
Recalling firm
ICU Medical, Inc.
Quantity
600 units
Product code
ONB
FDA submissions
K131549
Distribution
Worldwide distribution: US (Nationwide) including states of: AK AL AR AZ CA CO CT DE FL GA IA ID IL KS KY LA MA MD MI MN MS MT NC NE NJ NM NV NY OH OK OR PA SD TN TX VA WA WY and OUS (foreign) to countries of: Canada, France, and Japan.

Product description

ICU Medical Oncology Transfer Kit w/ChemoClave and ChemoLock Port; Spiros w/Red Cap; ChemoLock Port REF: CL4138

Code information (models, lots, serial numbers)

UDI:10887709096131/Lot: 14393176

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Other devices under the same FDA submission

90 devices cleared under K131549 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 97583).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page