FDA Drug recall D-1433-2012
Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art
- FDA Drug
- Class II
- terminated
- Published 2012-08-08
On 2012-08-08 the FDA classified a Class II recall of Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art by Bayer Healthcare Pharmaceuticals, citing cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1433-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-05-08 |
| Published | 2012-08-08 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bayer Healthcare Pharmaceuticals |
| Distribution | CA, KS |
Product
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.
Reason
Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.
Identifiers
| code_info | Lot Number: 81202450, Exp 06/15/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1433-2012%22
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