FDA recall record

Fresenius Medical Care Holdings AquaBplus Water Purification System, Part Number 24-2000-0 recall — FDA Z-1364-2022

AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US Installation Guideline instructed that 3-ring mains, instead of 2-ring mains,…

Class IIclassification
Z-1364-2022official record ID
Jul 20, 2022report date

Recall record at a glance

Official recordZ-1364-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateJul 20, 2022
Recall initiation dateAug 3, 2021
Quantity2 units
LocationWaltham, MA, United States

Official product description

AquaBplus Water Purification System, Part Number 24-2000-0, AquaBplus 2500 - Typ USA (G02040108-US), AquaBplus 2000 - Typ USA (G02040114-US), AquaBplus HF -Typ USA (G02040120FMC-US)

Why the product was recalled

AquaBplus HF module on the AquaBplus 2000 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 2000 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 NC and WV.

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: Telephone.

What to do next

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About this record

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