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Cardinal Health 200, LLC recalls

Every recall we track for Cardinal Health 200, LLC — 283 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 4 are rated “stop using now”.

283recalls

Recalls per year, by danger level

Recalls from Cardinal Health 200, LLC fell by more than half in 2025 (17, down from 37 in 2024). 1% rated “stop using now”.

2017: 4 recalls — 4 lower risk420172018: 25 recalls — 9 use caution, 16 lower risk2520182019: 26 recalls — 5 use caution, 21 lower risk2620192020: 20 recalls — 10 use caution, 10 lower risk2020202021: 40 recalls — 2 stop using now, 9 use caution, 29 lower risk4020212022: 40 recalls — 40 lower risk4020222023: 45 recalls — 13 use caution, 21 lower risk, 11 not yet rated4520232024: 37 recalls — 1 stop using now, 7 use caution, 28 lower risk, 1 not yet rated3720242025: 17 recalls — 1 stop using now, 9 use caution, 7 lower risk1720252026 (to date): 29 recalls — 2 use caution, 21 lower risk, 6 not yet rated292026to date

All FDA recall records for Cardinal Health 200, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Cardinal Health 200, LLC, by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700404
20180916025
20190521026
202001010020
20212929040
20220040040
2023013211145
20241728137
2025197017
2026 (to date)0221629

Most common reasons for Cardinal Health 200, LLC recalls

  • The suction valve may not close properly which could cause continuous suction.11
  • Demonstrated recognition and compatibility issues with syringe infusion pumps.6

What to do if you have a recalled Cardinal Health 200, LLC product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Cardinal Health 200, LLC recalls

60 shown

Cardinal Health 200, LLC recall questions

How many recalls has Cardinal Health 200, LLC had?

283 recalls from Cardinal Health 200, LLC are on record with U.S. safety agencies, from 2017–2026 (282 medical device, 1 drug).

What is the most recent Cardinal Health 200, LLC recall?

Cardinal Health 200, LLC recalls Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085, dated Aug 19, 2026. Every Cardinal Health 200, LLC recall is listed on this page, newest first.

Why are Cardinal Health 200, LLC products recalled?

The most common reasons on record: The suction valve may not close properly which could cause continuous suction. (11); Demonstrated recognition and compatibility issues with syringe infusion pumps. (6).

What should I do if I have a recalled Cardinal Health 200, LLC product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Cardinal Health 200, LLC recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.