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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71152

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

Open FDA event record

Event summary

Timeline bucket
April 10, 2015
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Oasis Medical, 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

ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Manufactured for OCULUS SURGICAL, Port St. Lucie, FL 34986, NDC 62144-5510-05

D-1084-2015
Recall number
D-1084-2015
Initiated
April 10, 2015
Classification
Class III
Status
Terminated
Recalling firm
Oasis Medical, Inc.
Quantity
9,731 cartons

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Failed pH specification

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed pH specification

Code information

Lot# V0814B, Exp 02/16; V1014H, Exp 04/16

Distribution pattern

FL