Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132734 |
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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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Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, N... | 2 | 02/09/2021 | Baxter Healthcare Corporation |
ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUI... | 2 | 10/16/2015 | Baxter Healthcare Corp |
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