Exact FDA event identifier

Event 83114

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

Event summary

Timeline bucket: May 10, 2019
Product types: Drug
Classifications: Class III
Statuses: Terminated
Recalling firm wording: Ecolab 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

QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 USA, NDC 47593-490-82

D-1393-2019

Recall number: D-1393-2019
Initiated: May 10, 2019
Classification: Class III
Status: Terminated
Recalling firm: Ecolab Inc
Quantity: 183 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.

Code information

Lot #: C040591, Exp 4/21

Distribution pattern

U.S.A. Nationwide