FDA applicant

Howard, Hills & Harsh

Salt Lake City, UT2 decisions1988–19880 recalls

FDA records 2 decisions for Howard, Hills & Harsh (Salt Lake City, UT) in 1988: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). No 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 Howard, Hills & Harsh’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Howard, Hills & Harsh since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Howard”

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

Howard Instruments, Inc. 5 Howard Medical Co. 3 Howard Associates, Inc. 3 Howard K. Mann & Assoc. 1 Howard N. Amos Design & Mfg. 1 Howard J. Nethery & Assoc. 1

Howard, Hills & Harsh

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Howard”