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CARDINAL HEALTH

Cardinal Health 200, LLC · Model 36-0319B · UDI-DI 10197106919743

OJV Prescription
0
510(k) clearances
6
Adverse events
38
Recalls
37
Facilities

Description

NEO NATAL CUT DOWN TRAY

Recalls

DateFirmReason
2017-09-20Merit Medical Systems, Inc.1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits.
2017-09-20Merit Medical Systems, Inc.2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product and placed into these dialysis kits.
2016-09-23Merit Medical Systems, Inc.Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
2016-09-23Merit Medical Systems, Inc.Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
2016-09-23Merit Medical Systems, Inc.Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
2016-09-23Merit Medical Systems, Inc.Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
2016-09-23Merit Medical Systems, Inc.Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
2010-12-22Medical Device Technologies, Inc.Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrit
2010-12-22Medical Device Technologies, Inc.Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrit
2010-12-22Medical Device Technologies, Inc.Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrit

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.