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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62651

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
May 08, 2012
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Bayer HealthCare Pharmaceuticals Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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.

D-1433-2012
Recall number
D-1433-2012
Initiated
May 08, 2012
Classification
Class II
Status
Terminated
Quantity
112.295 kg

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Number: 81202450, Exp 06/15/16

Distribution pattern

Kansas and California.

Field note

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