FDA recall record

Fresenius Medical Care Holdings AquaBplus and AquaBplus B2 Water Purification System recall — FDA Z-1536-2021

AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US Installation Guideline instructed that 3-ring mains, instead of 2-ring mains,…

Class IIclassification
Z-1536-2021official record ID
May 19, 2021report date

Recall record at a glance

Official recordZ-1536-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateMay 19, 2021
Recall initiation dateMar 18, 2021
Quantity27 units
LocationWaltham, MA, United States

Official product description

AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to remove organic and inorganic substances and microbial contaminants from the water used for hemodialysis or related therapies. Fresenius P/N 24-2500-0 All 3 units make up the AquaBplus 2500Fresenius Part Number: G02040109-US AquaBplus 3000 - Typ USA G02040115-US AquaBplus 2500 - Typ USA G02040120FMC-US AquaBplus HF- Typ USA

Why the product was recalled

AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US Installation Guideline instructed that 3-ring mains, instead of 2-ring mains, may be installed in combination with an AquaBplus 2500 device. The 3-ring main and fluid fly loops the heat disinfection may not be as effective as a 2-ring main installation

Distribution information

US Nationwide distribution in the states of FL, MA, MD, MI, MO, NC, NJ, NY, PA, PR, SC, TN, TX.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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