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April 20, 2009, 12:16:59 PMby recalls-bot |
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April 20, 2009, 12:16:59 PM by recalls-bot |
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99 Views |
April 19, 2009, 11:16:12 AM by recalls-bot |
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156 Views |
April 18, 2009, 09:11:37 AM by recalls-bot |
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140 Views |
April 18, 2009, 09:11:37 AM by recalls-bot |
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108 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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110 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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91 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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109 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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87 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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113 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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130 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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99 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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138 Views |
April 18, 2009, 07:01:17 AM by recalls-bot |
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103 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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Food and Drug Administration(FDA) has classified the voluntary medical device recall initiated on February 2, 2009 by Arrow International'">Arrow International Announces Worldwide Voluntary Recall of Intra Aortic Balloon Pump (IAB) Catheters (April 13)
Started by recalls-bot |
0 Replies
96 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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0 Replies
113 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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0 Replies
134 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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101 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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0 Replies
137 Views |
April 18, 2009, 07:01:16 AM by recalls-bot |
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