ICU Medical recalls specific oncology kits with a molding defect that may cause small leakage when inactivated. Affected kits include REF CL3960 with lot 5125262. Consumers should contact the manufacturer for details.
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
ICU Medical is recalling a specific oncology kit model that may leak small amounts of fluid due to a molding defect. This could cause issues during medical treatments if the kit is used improperly.
The molding defect in the kit can cause small amounts of leakage when the device is in the inactivated position. This leakage could potentially lead to fluid exposure or contamination during medical procedures.
Patients receiving chemotherapy treatments using the recalled oncology kit are most at risk. Healthcare providers using the kit for medical administration may also be affected.
Check for the product name 'REF CL3960 Oncology Kit' with the lot number 5125262. The kit includes a ChemoLock Port, Clamp, and Anti-Siphon Valve.
Reach out to ICU Medical for specific instructions on how to handle the recalled kit.
The recall indicates a potential for small leakage due to a molding defect, but the risk is low as it does not cause serious injury in normal use.
Contact ICU Medical directly for instructions on handling the recalled kit, as the remedy is not specified in the recall notice.
Check for the product name 'REF CL3960 Oncology Kit' with the lot number 5125262. The kit includes a ChemoLock Port, Clamp, and Anti-Siphon Valve.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1574-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1574-2021 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
