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U.S. Department of Health and Human Services

Medical Device Recalls
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231 to 240 of 500 Results *
Recall Date to: 07/14/2014
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Product Description
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FDA Recall
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ANSPACH***REF 98-0008***7cm Medium Attachment Custom***Rx Only*** This device is intended to be u... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used ... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0003***Sagittal microSaw Attachment Custom***Rx Only*** This device is intended ... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***eMax2 Lower Profile Foot Pedal***Rx Only*** This device is intended to be used with Ans... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0001***eMax Hand Control***Rx Only*** This device is intended to be used with An... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***Custom MCA5-1SD with Extended Exposure***Rx Only*** This device is intended to be used ... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0043***Custom Device eMax 2 Plus Hand Control that will work with a Speed Reducer**... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0044***Custom Device Speed Reducer with Bumper***Rx Only*** This device is inten... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0048***Custom Circular ePLUS-FP***Rx Only*** This device is intended to be used ... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***Custom QD11 Attachment with thinner nose tube***Rx Only*** This device is intended to b... 2 06/25/2014 The Anspach Effort, Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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