Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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Z-2282-2016 - Instructions for Use (IFU) for Progesterone 3 Calibrator Set, repackaged as one set/package. The Instructions for Use (IFU) included in the package was for the incorrect lot number. Only the IFU... | 3 | 07/25/2016 | Tosoh Bioscience, Inc. |
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