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U.S. Department of Health and Human Services

Medical Device Recalls

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201 to 210 of 210 Results
Product Code: DZE
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Product Description
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Recall
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FDA Recall
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EP Healing Abutment- An abutment device is a premanufactured prosthetic component directly connected... 2 10/21/2004 FEI # 1038806
Implant Innovations, Inc.
Biovent Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Microvent Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Swedevent Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Swissplus Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Taperlock Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Advent Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Screwvent Implant Line 2 07/23/2004 FEI # 1038806
Zimmer Dental Inc
Products are surgical drills packaged separately or included in a surgical kit so two products will ... 2 06/17/2003 FEI # 1038806
Implant Innovations, Inc.
Product is a drill used in dental surgery labeled in part: OFDR8 OsseoFix Drill 8mm Length 3i Impla... 2 06/17/2003 FEI # 1038806
Implant Innovations, Inc.
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