510(k) Report

FDA applicant

Sunbeam-Oster Household Products

Hattiesburg, MS1 decision1997–19970 recalls

FDA records 1 decision for Sunbeam-Oster Household Products (Hattiesburg, MS) in 1997: 1 510(k) clearance. All are in product code FRF (Cleaner, Air, Medical Recirculating). 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 Sunbeam-Oster Household Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sunbeam-Oster Household Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sunbeam-Oster Household Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Sunbeam-Oster”

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