FDA applicant

Procter & Gamble Mfg. Co.

Mchenry, IL72 decisions1976–19880 recalls

FDA records 72 decisions for Procter & Gamble Mfg. Co. (Mchenry, IL) from 1976 to 1988: 72 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and HHD (Pad, Menstrual, Unscented). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Procter & Gamble Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Procter & Gamble Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Procter & Gamble Mfg. Co. 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 “Procter”

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

Procter & Gamble Co. 33

Procter & Gamble Mfg. Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Procter”