FDA recall record

Fresenius Medical Care Holdings phosLo (calcium acetate) GelCaps, 667 mg, 200-count bottle recall — FDA D-1343-2014

Cross Contamination with Other Products: Potential for contaminant on the cotton packaging inside the bottle. Chemical analysis of the contaminant found…

Class IIclassification
D-1343-2014official record ID
May 28, 2014report date

Recall record at a glance

Official recordD-1343-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFresenius Medical Care Holdings, Inc.
Report dateMay 28, 2014
Recall initiation dateApr 14, 2014
Quantity14,496 bottles
LocationWaltham, MA, United States

Official product description

phosLo (calcium acetate) GelCaps, 667 mg, 200-count bottle, Rx only, Manufactured for Fresenius Medical Care North America, Waltham, MA 02451, NDC 0781-2081-02

Why the product was recalled

Cross Contamination with Other Products: Potential for contaminant on the cotton packaging inside the bottle. Chemical analysis of the contaminant found on the cotton was identified as a formulation of 4% Trimipramine methanesulfonate - a tricyclic antidepressant..

Distribution information

PA

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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