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U.S. Department of Health and Human Services

Medical Device Recalls
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81 to 90 of 500 Results *
Recall Date to: 04/21/2014
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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MedStream Refill Kit, U.S (6 units): 91-4288 Product Usage: The Medstream programmable pump is i... 1 09/30/2013 Codman & Shurtleff, Inc.
MedStream Refill Kit, U.S: 91-4287 Product Usage: The Medstream programmable pump is intended fo... 1 09/30/2013 Codman & Shurtleff, Inc.
MedStream Programmable Pump; 40ml - 91-4201US Usage: The Medstream programmable pump is intended... 1 09/30/2013 Codman & Shurtleff, Inc.
MedStream Programmable Pump; 20ml - 91-4200US Product Usage: The Medstream programmable pump is ... 1 09/30/2013 Codman & Shurtleff, Inc.
Product Name: AVEA® Ventilator. All Models. The affected devices are cleared under K073069 pm 1/2... 1 09/27/2013 Carefusion 211 Inc dba Carefusion
Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia breathing circuit is a d... 1 09/27/2013 King Systems Corp.
Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulat... 1 09/13/2013 B Braun Medical, Inc.
Microscan plus Negative Breakpoint Combo 4 Sold outside of US only. Product Usage: MicroScan®... 1 09/11/2013 Siemens Healthcare Diagnostics, Inc.
MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan® Synergies plus®... 1 09/11/2013 Siemens Healthcare Diagnostics, Inc.
Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: MicroScan® Synergies plus... 1 09/11/2013 Siemens Healthcare Diagnostics, Inc.

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