WalkMed Infusion, LLC
5 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes recall (Z-2219-2016) | WalkMed Infusion, LLC | 2016-07-18 |
| The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes recall (Z-2220-2016) | WalkMed Infusion, LLC | 2016-07-18 |
| Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietar recall (Z-0242-2016) | WalkMed Infusion, LLC | 2015-11-06 |
| Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infu recall (Z-1122-2014) | WalkMed Infusion, LLC | 2014-03-03 |
| WalkMed Triton Pole Mount Infusion Pump, Catalog 300000. Indicated for delivering infusion recall (Z-0307-2011) | Walkmed Infusion LLC | 2010-11-05 |
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Every clearance here is in the API, with alerts when new ones post.