Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-1024-04 - Percutaneous Transluminal Coronary Angioplasty system in sterile pouch. | 2 | 07/20/2004 |
FEI # 3001452571 Medtronic Vascular |
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