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CARDINAL HEALTH
Cardinal Health 200, LLC · Model 08-8060G · UDI-DI 10197106912423
OJV
Prescription
0
510(k) clearances
6
Adverse events
38
Recalls
37
Facilities
Description
LACERATION TRAY
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-09-20 | Merit Medical Systems, Inc. | 1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits. |
| 2017-09-20 | Merit Medical Systems, Inc. | 2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product and placed into these dialysis kits. |
| 2016-09-23 | Merit Medical Systems, Inc. | Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier. |
| 2016-09-23 | Merit Medical Systems, Inc. | Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier. |
| 2016-09-23 | Merit Medical Systems, Inc. | Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier. |
| 2016-09-23 | Merit Medical Systems, Inc. | Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier. |
| 2016-09-23 | Merit Medical Systems, Inc. | Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier. |
| 2010-12-22 | Medical 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 |
| 2010-12-22 | Medical 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 |
| 2010-12-22 | Medical 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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Get your free API keyRead the docsData 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.