Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K002803 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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O'Neil Sterile Field Intermittent Urinary Catheter Kit labeled in mart:"***ORIGINAL CLOSED SYSTEM BY... | 2 | 10/21/2011 | Go Medical Industries Pty., Ltd. |
O'Neil Sterile Field Intermittent Urinary Catheter Kit labeled in mart:"***ORIGINAL CLOSED SYSTEM BY... | 2 | 10/21/2011 | Go Medical Industries Pty., Ltd. |
O'Neil Sterile Field Intermittent Urinary Catheter Kit labeled in mart:"***ORIGINAL CLOSED SYSTEM BY... | 2 | 10/21/2011 | Go Medical Industries Pty., Ltd. |
O'Neil Sterile Field Intermittent Urinary Catheter Kit labeled in mart:"***ORIGINAL CLOSED SYSTEM BY... | 2 | 10/21/2011 | Go Medical Industries Pty., Ltd. |
O'Neil Sterile Field Intermittent Urinary Catheter Kit labeled in mart:"***ORIGINAL CLOSED SYSTEM BY... | 2 | 10/21/2011 | Go Medical Industries Pty., Ltd. |
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