FDA applicant

Reed Products, Inc.

Walker, MI4 decisions1984–19840 recalls

FDA records 4 decisions for Reed Products, Inc. (Walker, MI) in 1984: 4 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and LRR (First Aid Kit With Drug). 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 Reed Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reed Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Reed 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 “Reed”

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

Reed Medical (Zhejiang) Co., Ltd. 1

Reed Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reed”