Exact FDA event identifier

Event 77397

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

Event summary

Timeline bucket: June 01, 2017
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: L. Perrigo Company

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

Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010. NDC 0113-2003-12

D-0887-2017

Recall number: D-0887-2017
Initiated: June 01, 2017
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 181,776 (units/eaches)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Defective Container: Carton is missing the tablet blister strip and tablet.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Container: Carton is missing the tablet blister strip and tablet.

Code information

Lot #: 6LV1114, 6LV1115, 6LV1116, 6MV0976, 6MV0977, Exp.04/18; 7AV1173, 7AV1175, 7AV1176, Exp.07/18.

Distribution pattern

Nationwide in the US and Canada