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-1325-2009 - TheraSphere Administration Set (Part Number K125914-034). TheraSphere is indicated for radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable Hepatocell... | 3 | 06/05/2009 | MDS Canada Inc. DBA MDS Nordion |
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