Use caution Medical device recall · FDA · Published August 19, 2026

Presource Packs with Microstream Components Risk of Delayed Treatment

Cardinal Health recalls 210 Presource Packs containing Medtronic Microstream components due to potential delays in treatment and risk of unintended extubation.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0079-2027Medical device Cardinal Health ›

Use caution until it’s fixed

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.

✎ GovInfoNow plain-language explainer

Cardinal Health is recalling 210 Presource Packs that include Medtronic Microstream components. These kits may cause delays in treatment or unintended extubation during medical procedures, potentially leading to respiratory failure. Read more at govinfonow.com/recall/1629585-cardinal-health-200-llc-recalls-presource-packs-containing-medtronic-microstream.

Source Summary by GovInfoNow · govinfonow.com/recall/1629585-cardinal-health-200-llc-recalls-presource-packs-containing-medtronic-microstream · Updated October 21, 2026 · FDA enforcement record: FDA #Z-0079-2027

Cite this page

“Presource Packs with Microstream Components Risk of Delayed Treatment.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1629585-cardinal-health-200-llc-recalls-presource-packs-containing-medtronic-microstream. Based on FDA recall #Z-0079-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0079-2027%22&limit=1).

Cardinal Health 200, LLC recalled Presource Packs containing Medtronic Microstream Components due to difficulty disconnecting the adapter from endotracheal tubes, which can cause respiratory failure or hypoxia. The Food and Drug Administration announced the Class II recall on August 19, 2026.

How to tell if you have it

Brand: Cardinal Health
Product: Presource Packs with Microstream Components
Catalog Numbers: AN23366084, AN23366085, AN2336608H, AN2336608J, OMSVM4166A, AN2336608G
Kit lots: 40711, 46520, 20866, 23139, 24264, 25795, 27111, 27899, 29023, 29488, 30527, 31037, 31698, 32777, 33326, 33461, 33624, 35231, 35535, 35689, 36554, 36600, 36825, 38327, 38891, 40511, 41864, 43975, 44933, 45972, 47547, 47897, 48088, 48528, 49440, 47765, 50521, 53221, 53929, 54565, 54644, 18464, 18569, 19224
Units affected: 210 total kits

The hazard

Kits contain Microstream components that may be difficult to disconnect from the patient's endotracheal tube. This issue can result in a delay to treatment and unintended extubation, potentially causing respiratory failure, hypoxia, aspiration, or low oxygen saturation.

Context

GovInfoNow's records show Cardinal Health 200, LLC has issued 59 other recalls since June 27, 2017. Recent similar product recalls include Medline Medical Kits Recall: Particulate Risk in Fluid Path (March 24, 2026), Medline Medical Kits Recall: Particulate in Fluid Path Risk (March 24, 2026), and B Braun Medical IV Sets Recall: Risk of Medication Backflow (October 29, 2025).

How to tell if you have this one

Check for Presource Packs with catalog numbers AN23366084, AN23366085, AN2336608H, AN2336608J, OMSVM4166A, or AN2336608G. These kits were sold with specific lot numbers and UDI-DI codes.

Brand
Cardinal Health
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Catalog Numbers
Identify the catalog numbers on the Presource Pack, such as AN23366084, AN23366085, AN2336608H, AN2336608J, OMSVM4166A, or AN2336608G.
Verify Kit Lot Numbers
Check the lot numbers listed in the recall, including specific ranges like 40711, 46520, and others.

How this recall unfolded

Recall timeline

FDA published this recall 56 days after the firm started it.

Aug 19, 2026Firm started the recall
Oct 2, 2026FDA classified it Class II
Oct 14, 2026Published in FDA’s Enforcement Report
Oct 21, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What lot numbers are affected?

Affected lot numbers include 40711, 46520, 20866, 23139, 24264, 25795, 27111, 27899, 29023, 29488, 30527, 31037, 31698, 32777, 33326, and others as listed in the recall.

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Link to this recall

<a href="https://govinfonow.com/recall/1629585-cardinal-health-200-llc-recalls-presource-packs-containing-medtronic-microstream">Presource Packs with Microstream Components Risk of Delayed Treatment (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-0079-2027 (August 19, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0079-2027 to see it in context.
Plain-language summary written by qwen3:4b on October 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.