FDA applicant

Astra Pharmaceutical Products, Inc.

Westborough, MA2 decisions1985–19900 recalls

FDA records 2 decisions for Astra Pharmaceutical Products, Inc. (Westborough, MA) from 1985 to 1990: 2 510(k) clearances. Most are in product codes CCT (Applicator (Laryngo-Tracheal), Topical…) and EJI (Syringe, Cartridge). 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, anesthesiology panel, where it files most

How often FDA has decided Astra Pharmaceutical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Astra Pharmaceutical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Astra Pharmaceutical 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 “Astra”

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

Astra Tech, Inc. 38 Astra Meditec AB 3 Astra Orthomed, Inc. 1

Astra Pharmaceutical Products, 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?

Other applicant names beginning “Astra”