FDA recall record

Bayer HealthCare Pharmaceuticals Medroxyprogesterone acetate, micronized (EP, USP) active recall — FDA D-807-2013

Failed Stability Specifications: Out of specification results for particle size were obtained at the 60 month test point.

Class IIIclassification
D-807-2013official record ID
Jul 24, 2013report date

Recall record at a glance

Official recordD-807-2013
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBayer HealthCare Pharmaceuticals Inc.
Report dateJul 24, 2013
Recall initiation dateJun 13, 2013
Quantity194.62 kg
LocationMorristown, NJ, United States

Official product description

Medroxyprogesterone acetate, micronized (EP, USP) active pharmaceutical ingredient, Rx only, packaged in 6.0 kg drums (labeled as 6,000 kg), Bayer Schering Pharma AG, D-13342 Berlin

Why the product was recalled

Failed Stability Specifications: Out of specification results for particle size were obtained at the 60 month test point.

Distribution information

NY, CA

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.