Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K040186 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ANSPACH***1.85mm x 16 mm Fluted Router for MRI***Rx Only*** This device is intended to be used wi... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
| ANSPACH***REF SP-3014-00***4mm Fluted Ball for MRI***Rx Only*** This device is intended to be us... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
| IMRI AIR CONTROL Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| IMRI MOTOR Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| IMRI SHORT ATTACHMENT Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| IMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
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