FDA applicant

Carwild Corp.

Mchenry, IL6 decisions1979–19922 recalls

FDA records 6 decisions for Carwild Corp. (Mchenry, IL) from 1979 to 1992: 6 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) and GDY (Gauze/Sponge, Internal, X-Ray Detectable). 2 recalls are 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 and plastic surgery panel, where it files most

How often FDA has decided Carwild Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Carwild Corp. since 2007.

Recalls per year

1in 2026

2007high 1 (2022) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Carwild Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Carwild Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?