FDA recall record

Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose, Low recall — FDA D-0608-2021

Temperature Abuse: Product exposed to temperature outside specified limits.

Class IIIclassification
D-0608-2021official record ID
Jun 16, 2021report date

Recall record at a glance

Official recordD-0608-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateJun 16, 2021
Recall initiation dateApr 28, 2021
Quantity39 cases
LocationWaltham, MA, United States

Official product description

DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose, Low magnesium, Low Calcium and attached stay safe Exchange set, packaged in a) 2500 mL (NDC 49230-209-94) and b) 2000mL, packs of 5 (NDC 49230-209-92) Fresenius Medical Care NA, Waltham, MA 02451,

Why the product was recalled

Temperature Abuse: Product exposed to temperature outside specified limits.

Distribution information

Nationwide within the United States

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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