FDA recall record

Bayer HealthCare Pharmaceuticals Estradiol Hemihydrate M20 EP/USP Powder recall — FDA D-1433-2012

Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.

Class IIclassification
D-1433-2012official record ID
Aug 8, 2012report date

Recall record at a glance

Official recordD-1433-2012
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBayer HealthCare Pharmaceuticals Inc.
Report dateAug 8, 2012
Recall initiation dateMay 8, 2012
Quantity112.295 kg
LocationWayne, NJ, United States

Official product description

Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art. No. 165811, Bayer Pharma AG, D-13342 Berlin.

Why the product was recalled

Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.

Distribution information

Kansas and California.

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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