Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K122842 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i is intended for use in conju... | 2 | 09/11/2017 |
FEI # 2020563 Toshiba American Medical Systems |
| DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD) | 2 | 08/31/2018 |
FEI # 2020563 Canon Medical System, USA, INC. |
| Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software version: v5.00ER005 Product... | 2 | 07/11/2019 |
FEI # 2020563 Canon Medical System, USA, INC. |
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