FDA applicant

Reprocessing Products Corp

Maple Grove, MN6 decisions1995–20130 recalls

FDA records 6 decisions for Reprocessing Products Corp (Maple Grove, MN) from 1995 to 2013: 6 510(k) clearances. Most are in product codes MSY (Strip, Test, Reagent, Residuals For Dialysate…) and LIF (Dialyzer Reprocessing System). 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 Reprocessing Products Corp’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Reprocessing”

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

Reprocessing Products Corporation (Rpc) 2

Reprocessing Products Corp

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 “Reprocessing”