Medical Device Recalls
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1 result found
510(K) Number: K072621 |
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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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| Cincinnati Sub Zero, Steri-Probe Temperature Probe, Esophageal/Rectal Temperature Probe, Part Numbe... | 2 | 01/11/2012 |
FEI # 1516825 Cincinnati Sub-Zero Products Inc |
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