Medical Device Recalls
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1 result found
510(K) Number: K023062 |
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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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GemStar Bolus Cord; a remote bolus cord and switch for use with GemStar 7 Therapy and Pain Managemen... | 2 | 04/26/2012 | Hospira Inc. |
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