Data / Medical devices / Set, Blood Transfusion / United States
FDA-registered makers of Set, Blood Transfusion in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Set, Blood Transfusion (product code BRZ). 7 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Set, Blood Transfusion
- Product code
- BRZ
- Country
- United States
Makers of Set, Blood Transfusion in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 3 | November 17, 2022 | 0 | 1 | 0 | api.fda.gov |
| Arteriocyte Medical Systems, Inc. | Hopkinton, MA, United States | Manufacturer | 1 | October 4, 2013 | 0 | 0 | 0 | api.fda.gov |
| Carefusion | San Diego, CA, United States | Specification developer | 1 | April 1, 2005 | 0 | 0 | 0 | api.fda.gov |
| Charter Medical, LLC | Winston Salem, NC, United States | Contract manufacturer, Manufacturer | 1 | August 15, 2000 | 0 | 0 | 0 | api.fda.gov |
| Douglas Medical Products, Inc | Mundelein, IL, United States | Complaint file establishment, Specification developer | 1 | June 4, 1992 | 0 | 0 | 0 | api.fda.gov |
| Ecomed Solutions, LLC | Lindenhurst, IL, United States | Complaint file establishment, Specification developer | 1 | April 10, 2009 | 0 | 0 | 0 | api.fda.gov |
| Fenwal, Inc. | Lake Zurich, IL, United States | Complaint file establishment, Specification developer | 1 | March 3, 2008 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.