FDA recall record

Fresenius Medical Care Holdings NaturaLyte Liquid Bicarbonate Concentrate, 6.4 liter bottle recall — FDA Z-1739-2014

Container cap may contain foreign material- 0.60% - 0.80% Manganese

Class IIIclassification
Z-1739-2014official record ID
Jun 18, 2014report date

Recall record at a glance

Official recordZ-1739-2014
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateJun 18, 2014
Recall initiation dateMay 1, 2014
Quantity12 bottles
LocationWaltham, MA, United States

Official product description

NaturaLyte Liquid Bicarbonate Concentrate, 6.4 liter bottle to be used with a hemodialysis unit; Part Number: 08-4000-LB. The concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates.

Why the product was recalled

Container cap may contain foreign material- 0.60% - 0.80% Manganese

Distribution information

Distributed in the state of MO.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

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

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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