Medical Device Recalls
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1 result found
510(K) Number: K940082 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Pacific Hemostasis ® Thromboplastin-DS, catalog #100354, packaged in 4 mL lypholyzed vials, 10 bottl... | 2 | 06/26/2015 | Fisher Diagnostics, A Company of Fisher Scientific LLC |
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