510(k) Report

FDA applicant

Carrom Healthcare, Inc.

Sardis, MS5 decisions1985–19860 recalls

FDA records 5 decisions for Carrom Healthcare, Inc. (Sardis, MS) from 1985 to 1986: 5 510(k) clearances. Most are in product codes FNL (Bed, Ac-Powered Adjustable Hospital) and FNJ (Bed, Manual). 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 Carrom Healthcare, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Carrom Healthcare, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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