Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K974025 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
Large Craniotome Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
19cm Attachment, Black Max Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
19CM ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
11.25CM ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
STANDARD CRANIOTOME, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
KEYLESS DRIVER, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
26.65CM ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
12.6CM TAPERED ATTACHMENT, BLACK MAX Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
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