Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K112893 |
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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 CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line... | 1 | 09/14/2022 | Baxter Healthcare Corporation |
Baxter CLEARLINK System Non-DEHP Three Lead Extension Set. 6.0" (15 cm), 1.0 mL, Luer Activated Valv... | 2 | 10/29/2013 | Baxter Healthcare Corp. |
A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit, 6.0", Vol. 1.0 mL, 2 Luer Activa... | 2 | 05/07/2013 | Baxter Healthcare Corp. |
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