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U.S. Department of Health and Human Services

Medical Device Recalls
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Recall Date to: 07/05/2015 PMA Number: P900033
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FDA Recall
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Integra Dermal Regeneration Template-TS Catalog number 32021 Catalog number 82021 2 03/06/2009 Integra LifeSciences Corp
Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm) , Sterile; Integra LifeSciences Cor... 3 09/20/2008 Integra LifeSciences Corp
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