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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73295

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

Open FDA event record

Event summary

Timeline bucket
December 17, 2015
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Virtus Pharmaceuticals, Llc

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

VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary Supplement, 30-count Softgel bottles, Rx, Manufactured for Vitrus Pharmaceuticals, LLC, Tampa, FL 33619, NDC 69543-224-30, UPC 369543224305

D-0801-2016
Recall number
D-0801-2016
Initiated
December 17, 2015
Classification
Class III
Status
Terminated
Quantity
688 bottles ( 20,640 softgel capsules)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective Delivery System: Product may contain leaking capsules.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Delivery System: Product may contain leaking capsules.

Code information

Lot #21506132; Exp. 05/17

Distribution pattern

Nationwide