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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 45 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Z-1895-2014 - ANSPACH***REF 98-0035***Custom eMax 2 Plus Motor with microMax Disconnect Sleeve***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1896-2014 - ANSPACH***REF 98-0037***Custom Device SC2102 with fast stop firmware***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1897-2014 - ANSPACH***Custom XMax Motor, Pneumatic***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1898-2014 - ANSPACH***REF 98-0042***XMax Motor with Custom Hose***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1899-2014 - ANSPACH***REF 98-0043***Custom Device eMax 2 Plus Hand Control that will work with a Speed Reducer***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1900-2014 - ANSPACH***REF 98-0044***Custom Device Speed Reducer with Bumper***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1901-2014 - ANSPACH***REF 98-0048***Custom Circular ePLUS-FP***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1902-2014 - ANSPACH***Custom QD11 Attachment with thinner nose tube***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1903-2014 - ANSPACH***REF-98-0056***Custom Device Autolube III modified with a swivel***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
Z-1904-2014 - ANSPACH***REF-98-0062***Custom Device eMax2 Plus Hand Control***Rx Only*** This device is intended to be used with Anspach Systems 2 06/25/2014 The Anspach Effort, Inc.
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