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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 42 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0229-2009 - PREMISE, PART NO. 32650, 10 PACK UNIDOSE PREMISE A1, dental composite 2 11/25/2008 Kerr Corp
Z-0270-2009 - PREMISE KIT, PART NO. 33882, UNIDOSE PREMISE MINI KIT, dental composite 2 11/25/2008 Kerr Corp
Z-0231-2009 - PREMISE, PART NO. 32652, 10 PACK UNIDOSE PREMISE A3, dental composite 2 11/25/2008 Kerr Corp
Z-0232-2009 - PREMISE, PART NO. 32653, 10 PACK UNIDOSE PREMISE A3.5, dental composite 2 11/25/2008 Kerr Corp
Z-0233-2009 - PREMISE, PART NO. 32654, 10 PACK UNIDOSE PREMISE A4, dental composite 2 11/25/2008 Kerr Corp
Z-0234-2009 - PREMISE, PART NO. 32655, 10 PACK UNIDOSE PREMISE B1, dental composite 2 11/25/2008 Kerr Corp
Z-0235-2009 - PREMISE, PART NO. 32656, 10 PACK UNIDOSE PREMISE B2, dental composite 2 11/25/2008 Kerr Corp
Z-0236-2009 - PREMISE, PART NO. 32657, 10 PACK UNIDOSE PREMISE B3, dental composite 2 11/25/2008 Kerr Corp
Z-0237-2009 - PREMISE, PART NO. 32658, 10 PACK UNIDOSE PREMISE B4, dental composite 2 11/25/2008 Kerr Corp
Z-0238-2009 - PREMISE, PART NO. 32659, 10 PACK UNIDOSE PREMISE C1, dental composite 2 11/25/2008 Kerr Corp
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