Medical Device Recalls
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1 to 10 of 28 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2842-2018 - DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2845-2018 - DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2846-2018 - BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2847-2018 - CombiDiagnost R90 (Stitching Patient Support) 709030 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2848-2018 - DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2841-2018 - DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2849-2018 - DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2850-2018 - DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2851-2018 - DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
| Z-2852-2018 - DigitalDiagnost 4.1 (Stitching Patient Support) 712225 | 2 | 08/17/2018 |
FEI # 3003768251 Philips Medical Systems Gmbh, DMC |
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