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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0609-2009 - DLP(R) Pericardial/Intracardiac Sump Cannulae, 20 Fr., P/N: 12112. This product is intended for draining the pericardial sac or the cardiac chambers. 2 01/26/2009 FEI # 1000116158
Medtronic Cardiovascular Revascularization & Surgical Therap
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