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Cardiopulmonary Bypass Catheter Kit

FDA product code OEU · Class 2 · Cardiovascular

4
Registered devices
1
Adverse events
3
Recalls
0
510(k) clearances

Devices with this code

CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLC

Recent recalls

DateFirmReason
2009-03-23Medtronic Cardiovascular Revascularization & Surgical TherapMedtronic has identified a small number of One Source Kits and MAXPAC/Total System lots with incorrect Use Before Dates on the outer kit package label. The Use
2009-03-23Medtronic Cardiovascular Revascularization & Surgical TherapMedtronic has identified a small number of One Source Kits and MAXPAC/Total System lots with incorrect Use Before Dates on the outer kit package label. The Use
2009-03-23Medtronic Cardiovascular Revascularization & Surgical TherapMedtronic has identified a small number of One Source Kits and MAXPAC/Total System lots with incorrect Use Before Dates on the outer kit package label. The Use

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.