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U.S. Department of Health and Human Services

Medical Device Recalls
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111 to 120 of 500 Results *
Recall Date to: 07/26/2014
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FDA Recall
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MedStream Programmable Pump; 20ml Pump EMEA 91-4200 Product Usage: The Medstream programmable pu... 1 09/30/2013 Codman & Shurtleff, Inc.
MedStream Programmable Pump; 40ml Pump EMEA 91-4201 Product Usage: The Medstream programmable pu... 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.
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 Refill Kit (1 unit), EMEA: 91-4289 Product Usage: The Medstream programmable pump is i... 1 09/30/2013 Codman & Shurtleff, Inc.
MedStream Refill Kit (6 units), EMEA: 91-4290 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.

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