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Cardinal Health 303 Inc DBA Alaris Products

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
U19 Socketed Integrated Circuit ("U19 IC") on the logic board of Alaris Pump modules (aka. recall (Z-1710-2008)Cardinal Health 303 Inc DBA Alaris Products2008-06-10
Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built recall (Z-1711-2008)Cardinal Health 303 Inc DBA Alaris Products2008-06-10
U9 Socket Integrated Circuit ("U9 IC") on the display board of the following Alaris System recall (Z-1712-2008)Cardinal Health 303 Inc DBA Alaris Products2008-06-10
Cardinal Health Alaris Pump Module (formerly Medley Pump Module), Model 8100, Cardinal Hea recall (Z-0460-2008)Cardinal Health 303 Inc DBA Alaris Products2008-01-04
Texium Closed Male Luer (CML), Model Number 10012241, Cardinal Health, SanDiego, CA. recall (Z-0218-2008)Cardinal Health 303 Inc DBA Alaris Products2007-11-08
Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Die recall (Z-0555-2007)Cardinal Health 303 Inc DBA Alaris Products2007-09-26
Alaris Medical Systems IV Administration Set, Low Sorbing Extension Set, Model C20014, Rx recall (Z-1078-2007)Cardinal Health 303 Inc DBA Alaris Products2007-08-03
All IV Administration Infusion Sets intended for use with the Gemini Infusion Pump and Ala recall (Z-1020-2007)Cardinal Health 303 Inc DBA Alaris Products2007-08-02
Alaris SE Pump (formerly Signature Edition Infusion Pump); Model Numbers: 7000, 7100, 7101 recall (Z-1484-06)Cardinal Health 303 Inc DBA Alaris Products2006-09-19

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Every clearance here is in the API, with alerts when new ones post.