FDA applicant

Retrax Safety Systems, Inc.

Miami, FL1 decision2000–20000 recalls

FDA records 1 decision for Retrax Safety Systems, Inc. (Miami, FL) in 2000: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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 Retrax Safety Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Retrax Safety Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Retrax Safety Systems, 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 “Retrax”

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

Retrax 2

Retrax Safety Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Retrax”