← Back to recall lookup
Device Class II · moderate Ongoing

Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085 AN2336608H AN2336608J Intubating Bag Kit Catalog Number OMSVM4166A Intubation UH Kit Catalog Number AN2336608G

Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a procedure. The issue can result in a delay to treatment and unintended extubation. The potential exists for respiratory failure, hypoxia, aspiration, or low oxygen saturation.

Recalling firmCardinal Health 200, LLC
ReasonKits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a procedure. The issue can result in a delay to treatment and unintended extubation. The potential exists for respiratory failure, hypoxia, aspiration, or low oxygen saturation.
Risk classClass II (Class II · moderate)
StatusOngoing
Report dateOct 14, 2026
InitiatedAug 19, 2026
RegionIL, United States
DistributionPending
Quantity210 total kits
Code/LotAN23366084 UDI-DI 10197106950074 Kit lot 40711 AN23366085 UDI-DI 10198956177987 Kit lot 46520 AN2336608H UDI-DI 10197106159828 Kit lots 20866 23139 24264 25795 27111 27899 29023 29488 30527 31037 316…
TypeVoluntary: Firm initiated
Recall numberZ-0079-2027

Official source

U.S. FDA — Recalls, Market Withdrawals & Safety Alerts fda.gov ↗

You can re-verify each item on the official FDA site using its recall number. (Recall number: Z-0079-2027)

openFDA (U.S. Food & Drug Administration) — food/drug/device enforcement · CC0 1.0 (public domain)

Find out more

The links above open external searches by recall number / product name; the results are the responsibility of each site.

This page summarizes U.S. FDA data for general information and is not medical advice. Confirm details via official FDA announcements and the manufacturer.