Medical Device Recalls
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11 to 12 of 12 Results
Recall Date to: 05/28/2015 510(K) Number: K980987 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Bard Ponsky PEG Safety System ''Pull'' Reorder Number: 001925 | 2 | 09/11/2003 | Bard Endoscopic Technologies |
Bard PEG Safety System ''Guidewire'' Reorder Number: 001928 | 2 | 09/11/2003 | Bard Endoscopic Technologies |
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