Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K000723 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Magic3 (Intermittent Catheter), Sterile. Uncoated 10 French Male Length REF 53310 Rochester Medical... | 2 | 03/16/2009 | Rochester Medical Corp |
Magic3 (Intermittent Catheter), Sterile. Hydrophilic 6 French Pediatric Length REF 52606 Rochester ... | 2 | 03/16/2009 | Rochester Medical Corp |
Magic3 (Intermittent Catheter), Sterile. Uncoated 10 French Pediatric Length REF 52310 Rochester Me... | 2 | 03/16/2009 | Rochester Medical Corp |
Magic3 (Intermittent Catheter), Sterile, Uncoated 6 French Pediatric Length REF # 52306 Rochester M... | 2 | 03/16/2009 | Rochester Medical Corp |
Magic3 (Intermittent Catheter), Sterile, Uncoated 8 French Pediatric Length REF 52308 Rochester Med... | 2 | 03/16/2009 | Rochester Medical Corp |
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