Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K082268 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| CAPNOSTREAM 20 (US) N, Part Number CS08651 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) M, Part Number CS08653 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) M W/PRINTER, Part Number CS08659 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) M W/PRINTER REFURBISHED, Part Number CS78659 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) M W/PRINTER TO MASIMO, Part Number CS08751 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US)M REFURBISHED, Part Number CS78653 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) N W/PRINTER REFURBISHED, Part Number CS78657 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
| Capnostream20 (US) M TO MASIMO, Part Number CS08750 | 2 | 10/03/2018 | Oridion Medical 1987 Ltd. |
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