Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172410 |
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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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smiths medical portex Loss of Resistance Device, REF 100/398/000 | 2 | 10/19/2021 | Smiths Medical ASD Inc. |
Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar pun... | 2 | 04/29/2020 | Smiths Medical ASD Inc. |
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