Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 07/25/2014 |
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Results per Page |
Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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Z-1641-2009 - In Situ Bender Cutter Kit Narrow Sterile, Catalog number 530.522S. Used with Synthes' Rapid Resorbable Fixation System which is intended for use in fracture repair and reconstructive procedures of ... | 2 | 05/21/2009 | Synthes Spine |
Z-1640-2009 - In Situ Bender Cutter Kit Wide Sterile, Catalog number 530.521S Used with Synthes' Rapid Resorbable Fixation System which is intended for use in fracture repair and reconstructive procedures of the... | 2 | 05/21/2009 | Synthes Spine |
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