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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71601

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

Open FDA event record

Event summary

Timeline bucket
June 26, 2015
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
VistaPharm, 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

METOCLOPRAMIDE ORAL SOLUTION, USP 10 mg/10 mL, 10 mL cups, Rx only. Manufactured by VistaPharm, Inc, Largo, FL. NDC: 66689-031-01.

D-1831-2015
Recall number
D-1831-2015
Initiated
June 26, 2015
Classification
Class III
Status
Terminated
Recalling firm
VistaPharm, Inc.
Quantity
84,100 Cups

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective Container: Lids on unit dose cups are not fully qualified.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Container: Lids on unit dose cups are not fully qualified.

Code information

Lot #: 387500, Expiry: 01/17

Distribution pattern

U.S. Including: CA, IL, LA, OH, PA, and SC.