Exact FDA event identifier

Event 87016

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

Event summary

Timeline bucket: December 30, 2020
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Allergan, PLC.

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

Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie company Madison, NJ 07940 UPC 3 00236 63410 0, NDC 0023-6634-10.

D-0233-2021

Recall number: D-0233-2021
Initiated: December 30, 2020
Classification: Class II
Status: Terminated
Recalling firm: Allergan, PLC.
Quantity: 100,634 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

Labeling: Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Missing instructions for use insert

Code information

Lots: T0392 Exp. Jul. 2022, T0843 Exp. Aug. 2022

Distribution pattern

Nationwide.