Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032144 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CE17TKFCPS EPIDURAL FULL TRAY, Material Number 332078 Connection device used by physicians to pr... | 2 | 10/01/2018 | B. Braun Medical, Inc. |
| CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY, Material Number 332077 Connection device used by physici... | 2 | 10/01/2018 | B. Braun Medical, Inc. |
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