Medical Device Recalls
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1 result found
Recall Number: Z-0361-2014 |
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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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| Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US) | 2 | 11/19/2013 |
FEI # 2916714 Aesculap, Inc. |
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