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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83114

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

Open FDA event record

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

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