Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K884505 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: Multiday lnfusor, Seven Day lnfusor and the Basal/Bolus lnfusor: Single day Infusor ... | 2 | 06/27/2013 | Baxter Healthcare Corp. |
| Brand Name: Basal/Bolus Infusor. Indicated for the intravenous administration of medications. | 2 | 06/27/2013 | Baxter Healthcare Corp. |
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