FDA applicant

Bethel Latex Products, Inc.

Haz;Ejirst, MS1 decision1991–19910 recalls

FDA records 1 decision for Bethel Latex Products, Inc. (Haz;Ejirst, MS) in 1991: 1 510(k) clearance. All are in product code LZB (Finger Cot). 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 Bethel Latex Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bethel Latex Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bethel”

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

Bethel, Inc. 1

Bethel Latex Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bethel”