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U.S. FDA openFDA (510(k) clearances and device enforcement reports). Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0079-2027%22

Class II recall Z-0079-2027: Cardinal Health 200, LLC

Q: How to monitor Class II recall Z-0079-2027: Cardinal Health 200, LLC and peer other records

FDAPulse lists new FDAPulse records from U.S. FDA openFDA (510(k) clearances and device enforcement reports) as they are published; a free weekly email digest and paid alerts follow Illinois records like this one.

Class II recall Z-0079-2027: Cardinal Health 200, LLC (Illinois): Cardinal Health 200, LLC. Dated 21 days ago, it is in the active follow-up window. Score 62/100. As of 2026-11-03, from U.S. FDA openFDA (510(k) clearances and device enforcement reports).

Data as of 2026-11-03 · Compiled by Zalwin from U.S. FDA openFDA (510(k) clearances and device enforcement reports)

Free preview: all 14 published fields of this record are shown below. Locked: 56 related IL FDAPulse records and the 5-column CSV export.

Field	Value
Record	Device recall
Recall number	Z-0079-2027
Recalling firm	Cardinal Health 200, LLC
Classification	Class II
Status	Ongoing
Voluntary / mandated	Voluntary: Firm initiated
Specialty	Other
Product	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
Reason	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.
Quantity	210 total kits
Distribution	Pending
Recall initiated	2026-08-19
Reported	2026-10-14
Firm location	Waukegan, IL, United States
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Source agency: U.S. FDA openFDA (510(k) clearances and device enforcement reports)
Record date: 2026-10-14
Data refreshed: 2026-11-03
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LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Tue, 03 Nov 2026 18:05:14 GMT

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Peer benchmark and outreach value: Class II recall Z-0079-2027: Cardinal Health 200, LLC and 57 Illinois peers

Your role Typical deal size (USD) Assumed reply-to-deal rate (%)

Illinois FDAPulse records like this one: 57
Timing: Medium: dated in the last 30 days
Estimated pipeline if you contact every Illinois peer: $11,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

62 / 100 Predicate Speed & CAPA Advisory Opportunity Score

Class II recall: usually triggers CAPA and quality-system remediation work.
Recall is still ongoing.
Posted 21 days ago.

What is the FDAPulse record for Class II recall Z-0079-2027: Cardinal Health 200, LLC in Illinois?

Class II device recall Z-0079-2027 by Cardinal Health 200, LLC: Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due repo

How does Class II recall Z-0079-2027: Cardinal Health 200, LLC compare to other Illinois FDAPulse records?

It is 21 days old, still within a typical 45-day follow-up window.

Class II recall Z-0079-2027 vs. top 2 peers

Organization	Location	Record date
Class II recall Z-0079-2027	IL	2026-10-14
Class II recall Z-0281-2027	IL	2026-10-28
Class II recall Z-0275-2027	IL	2026-10-28

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