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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 63285

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 01, 2012
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Dr. Reddy's Laboratories, 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

3 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 3

Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-30

D-178-2013
Recall number
D-178-2013
Initiated
August 01, 2012
Classification
Class II
Status
Terminated
Quantity
27,805 bottles

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Chemical Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

Code information

Lot #: C201028, Exp 12/13

Distribution pattern

Nationwide

drug · product 2 of 3

Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30

D-179-2013
Recall number
D-179-2013
Initiated
August 01, 2012
Classification
Class II
Status
Terminated
Quantity
86, 093 bottles

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Chemical Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

Code information

Lot #: C201922, Exp 1/14

Distribution pattern

Nationwide

drug · product 3 of 3

Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30

D-180-2013
Recall number
D-180-2013
Initiated
August 01, 2012
Classification
Class II
Status
Terminated
Quantity
48, 754 bottles (C108376)/47,520 bottles (C108634)

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Chemical Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

Code information

Lot #: C108376, C108634, Exp 11/13

Distribution pattern

Nationwide