FDA recall record

Fresenius Medical Care Delflex Peritoneal Dialysis Solution with 1.5% Dextrose, LM/LC recall — FDA D-0389-2021

Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

Class IIclassification
D-0389-2021official record ID
May 26, 2021report date

Recall record at a glance

Official recordD-0389-2021
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFresenius Medical Care, North America
Report dateMay 26, 2021
Recall initiation dateApr 14, 2021
Quantity709 cases
LocationOgden, UT, United States

Official product description

Delflex Peritoneal Dialysis Solution with 1.5% Dextrose, LM/LC, packaged in a case containing 2 x 6 Liter bags, Rx only, NDC 49230-206-60, Fresenius Medical Care North America, Waltham, MA 02451

Why the product was recalled

Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

Distribution information

USA Nationwide

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

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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