Medical Device Recalls
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1 result found
Recall Number: Z-0809-2018 |
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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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| proSA Tool Set used to adjust and verify the proSA Adjustable Shunt System Shunt, central nervous... | 2 | 03/01/2018 |
FEI # 2916714 Aesculap Implant Systems LLC |
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