FDA applicant

Baxter Corp.

Round Lake, IL1 decision1994–19941 recall

FDA records 1 decision for Baxter Corp. (Round Lake, IL) in 1994: 1 510(k) clearance. All are in product code FRN (Pump, Infusion). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Baxter Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Baxter Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Baxter Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Baxter”

FDA records each applicant name separately; these may or may not be the same firm.

Baxter Healthcare Corp 574 Baxter Diagnostics, Inc. 72 Baxter Edwards 11 Baxter Bentley Laboratories, Inc. 3 Baxter Healthcare Corportation 3 Baxter Healthcare Corporation - Renal Division 2 Baxter/ Synovis Micro Companies Alliance, Inc. 2 Baxter Healthcare Corp/ Excel Medical 1 Baxter Centre For Medical Research 1 Baxter Healthcare Corproration 1 Baxter Interwoven Offsite 1 Baxter Healthcare Corp., Bioscience 1

Baxter Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Baxter”