FDA applicant

Rexam Medical Packaging, Inc.

Mundelein, IL2 decisions1996–19970 recalls

FDA records 2 decisions for Rexam Medical Packaging, Inc. (Mundelein, IL) from 1996 to 1997: 2 510(k) clearances. All are in product code KCT (Sterilization Wrap Containers, Trays…). 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 Rexam Medical Packaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rexam Medical Packaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rexam Medical Packaging, 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 “Rexam”

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

Rexam Consummer Plastics Inc.D/B/A Rexam Pharma 1 Rexam Pharma 1 Rexam Healthcare 1

Rexam Medical Packaging, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rexam”