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Bivona

ICU MEDICAL, INC. · Model XU25HS25NGE057N · UDI-DI 10887709166360

JOH Prescription

510(k) clearances

14,926

Adverse events (164 deaths)

131

Recalls

Facilities

Description

XU25HS25NGE057N Bivona DI: Non-Adjustable-Wired_Non-Sterile

Recalls

Date	Firm	Reason
2026-04-15	Covidien LLC	Due to customer complaint regarding incorrect display box labeling.
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2025-02-26	Covidien	Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspeci
2023-08-22	Smiths Medical ASD Inc.	The unit box is labeled with an incorrect expiration date (the manufacturing date of 3/17/2021) but the individual packaging contains the correct expiration date (3/17/2026).
2023-04-07	Cook Incorporated	There were reports from customers that the tracheostomy in the sets and trays is not making a secure connection with the 15mm cap and other 15mm circuit components and accessories.
2023-04-07	Cook Incorporated	There were reports from customers that the tracheostomy in the sets and trays is not making a secure connection with the 15mm cap and other 15mm circuit components and accessories.
2023-03-24	Covidien	A manufacturing error, resulted in a less than specified diameter of adult flexible tracheostomy tube connectors, which results in unsecure connections with 15mm caps and other 15m

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.