Medical Device Recalls
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1 to 10 of 22 Results
510(K) Number: K955084 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ***REF BLACKMAX-N***Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort, Inc. Intended for ... | 2 | 01/09/2014 |
FEI # 1045834 The Anspach Effort, Inc. |
| 10.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 11CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 13.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 14CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 16.5CM MICRO REVISION ATTACH, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 16CM MIN INVASIVE ATTACH, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 22CM MICRO REVISION ATTACH, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 45 degree Contra Angle Attachment Product Usage: Pneumatic system | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
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