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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 04/03/2014
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Product Description
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FDA Recall
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Z-0619-2008 - Allogenix; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: 02-3110, Interpore Cross International, a Biomet company (Allogenix DBM products contain human tissue (allograft bone) and are ... 3 02/14/2008 Interpore Cross International Inc
Z-0618-2008 - InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005, DBM010, DBMW05 & DBMW10, Interpore Cross International, a Biomet company (lnterGro DBM products contain hu... 3 02/14/2008 Interpore Cross International Inc
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