FDA applicant

E. R. Squibb & Sons, Inc.

New York, NY32 decisions1977–19820 recalls

FDA records 32 decisions for E. R. Squibb & Sons, Inc. (New York, NY) from 1977 to 1982: 32 510(k) clearances. Most are in product codes EXB (Collector, Ostomy) and CDP (Radioimmunoassay, Total Triiodothyronine). 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, gastroenterology and urology panel, where it files most

How often FDA has decided E. R. Squibb & Sons, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E. R. Squibb & Sons, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — E. R. Squibb & Sons, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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E. R. Squibb & Sons, Inc.

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?