Medical Device Recalls
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1 result found
510(K) Number: K990236 |
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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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ProtectIV® Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton. | 2 | 11/08/2019 | Smiths Medical ASD Inc. |
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