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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 500 Results *
Recall Date from: 01/01/2016 Recall Date to: 06/13/2016
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Product Description
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Class
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FDA Recall
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MED-RX Single Use REF 54-3680R, 8 FR. x 36" (91CM) Polyurethane Feeding Tube For Pediatric Use with ... 2 01/06/2016 Benlan, Inc.
Oncentra External Beam - VMAT - Radiation therapy planning system Product Usage: The Oncentra sy... 2 01/07/2016 Elekta, Inc.
Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to be used for calibration of ... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended to be used for calibration o... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of th... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to be used for calibration of th... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in vitro diagnostic 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care CKMB DilPak- an in vitro diagnostic product intended to be used in conjunction wi... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the measurement of cardiac troponin I ... 2 01/07/2016 Siemens Healthcare Diagnostics Inc
Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-term... 2 01/07/2016 Siemens Healthcare Diagnostics Inc

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