FDA applicant

Ansell Pacific, Inc.

Tucson, AZ2 decisions1989–19890 recalls

FDA records 2 decisions for Ansell Pacific, Inc. (Tucson, AZ) in 1989: 2 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 Ansell Pacific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ansell Pacific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ansell Pacific, 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 “Ansell”

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

Ansell Healthcare Products, LLC 36 Ansell, Inc. 30 Ansell Perry 22 Ansell Intl. 4 Ansell Healthcare, Inc. 3 Ansell Edmont Industrial, Inc. 2 Ansell Heathcare Products, LLC 1 Ansell Malaysia Sdn Bhd 1

Ansell Pacific, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ansell”