Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0659-03 - TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016. | 2 | 03/20/2003 |
FEI # 1000160576 Interpore Cross International Inc |
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