Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K790312 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100... | 1 | 03/12/2025 | Smiths Medical ASD, Inc. |
| 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubation... | 1 | 08/28/2014 | Smiths Medical ASD, Inc. |
| H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy,15mm Conn, Holder Pediatric Endotracheal Intuba... | 1 | 08/28/2014 | Smiths Medical ASD, Inc. |
| H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubatio... | 1 | 08/28/2014 | Smiths Medical ASD, Inc. |
| H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy, 15mm Conn, Holder Pediatric Endotracheal Intuba... | 1 | 08/28/2014 | Smiths Medical ASD, Inc. |
| Portex Low Dead Space Connector with Sideport, 3.5mm Product Usage: The connector is used to att... | 1 | 06/11/2014 | Smiths Medical ASD, Inc. |
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