FDA applicant

Globe Safety Products, Inc.

N.T. Hong Kong, GB2 decisions1977–19890 recalls

FDA records 2 decisions for Globe Safety Products, Inc. (N.T. Hong Kong, GB) from 1977 to 1989: 2 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and BYE (Attachment, Breathing, Positive End Expiratory…). 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 Globe Safety Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Globe Safety Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Globe”

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

Globe Ent., Inc. 5 Globe Management Support, Inc. 2 Globe Safety Equipment, Inc. 1

Globe Safety Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Globe”