Medical Device Recalls
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11 to 13 of 13 Results
Recall Date to: 09/18/2014 PMA Number: P970018 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer c... | 2 | 07/26/2012 | Tripath Imaging, Inc. |
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation ... | 2 | 07/26/2012 | Tripath Imaging, Inc. |
BD PrepStain System, Model Number: 799-14000-00; Catalog Number: 05CR000021, 05CR00021R, 799-13000-0... | 2 | 03/19/2009 | Bd Diagnostic Systems Tripath |
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