Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133404 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument softw... | 2 | 01/12/2015 | Phadia US Inc |
| Phadia 1000 Instrument, Article Number 12-3800-01. | 2 | 01/18/2018 | Phadia US Inc |
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