# FDA device recall: Bicarby" Dialysate;  Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;

> recall · VERIFIED · 2026-05-12

Firm: Fresenius Medical Care Holdings, Inc. · Class II · Given the increased number of leaks reported by  users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during m

- Company: Fresenius Medical Care Holdings, Inc.
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.