Medical Device Recalls
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1 result found
510(K) Number: K961552 |
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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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18 Gauge thin wall needle as part of a Central Venous Catheter Kit | 2 | 02/24/2004 | Abbott Laboratories HPD/ADD/GPRD |
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