FDA recall record

Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, 5000 mL recall — FDA D-1610-2014

Presence of Particulate Matter: particulate matter was found during the manufacturing process.

Class Iclassification
D-1610-2014official record ID
Oct 8, 2014report date

Recall record at a glance

Official recordD-1610-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmBaxter Healthcare Corp.
Report dateOct 8, 2014
Recall initiation dateAug 7, 2014
Quantity50,530 bags
LocationDeerfield, IL, United States

Official product description

Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, 5000 mL Ambu-Flex II container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Product Code L5B5202, NDC 0941-0457-05.

Why the product was recalled

Presence of Particulate Matter: particulate matter was found during the manufacturing process.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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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