Exact FDA event identifier

Event 79267

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

Event summary

Timeline bucket: February 15, 2018
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Medline Industries 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

PVP Scrub Solution, Povidone Iodine, 7.5% (equivalent to 0.75% available iodine), 4 FL OZ bottle, Manufactured in USA by Medline Industries, Inc., Northfield, IL 60093; Product Number MDS093945; NDC 53329-938-04

D-0546-2018

Recall number: D-0546-2018
Initiated: February 15, 2018
Classification: Class II
Status: Terminated
Recalling firm: Medline Industries Inc
Quantity: 67,104 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.

Code information

Lot #: 16EJ0023, Exp 04/18

Distribution pattern

Nationwide in the USA and Curacao