Exact FDA event identifier

Event 62887

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

Event summary

Timeline bucket: January 19, 2011
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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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 5 mg/5 mL, This cup delivers 10 mL, Rx Only, Manufactured by VistaPharm, Inc., Largo FL33771

D-1669-2012

Recall number: D-1669-2012
Initiated: January 19, 2011
Classification: Class III
Status: Terminated
Recalling firm: VistaPharm, Inc.
Quantity: 73,800 cups

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"

Code information

195900 exp. 01/12.

Distribution pattern

Nationwide