Reported Oct 14, 2026 · Ongoing · Updated Oct 20, 2026

Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085…

Cardinal Health 200, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

  • Presource Packs containing
  • Medtronic Microstream ComponentsIntubation Kit Catalog Numbers AN23366084 AN23366085 AN2336608H AN2336608J Intubating Bag Kit Catalog Number OMSVM4166A Intubation UH Kit Catalog Number AN2336608G
Lot codes and dates
  • AN23366084 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
    • 31698
    • 32777
    • 33326
    • AN2336608J
    UDI-DI 10197106704035 Kit lots
    • 33461
    • 33624
    • 35231
    • 35535
    • 35689
    • 36554
    • 36600
    • 36825
    • 38327
    • 38891
    • 40511
    • 41864
    • 43975
    • 44933
    • 45972
    • 47547
    • 47897
    • 48088
    • 48528
    • 49440
    • OMSVM4166A
    UDI-DI 10198956162259 Kit Lots 47765 50521 53221 53929 54565 54644 AN2336608G UDI-DI 10197106052105 Kit lots 18464 18569 19224
Amount recalled
210 total kits

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 12:27 AM UTC

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