Quik-care Solution
FDA Recall NDC 47593-490
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with Quik-care (NDC 47593-490). A significant event, classified as Class III, was initiated on May 10, 2019 by Ecolab Inc.. The reported reason for this action was: "Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material."
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
Reported Recall Events
Class III Terminated
Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
May 10, 2019
Jun 26, 2019
183 cases
Recall Profile & Regulatory Data
Event ID
83114
Classification
Class III
Enforcement Status
Terminated
Recalling Firm
Ecolab Inc
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
U.S.A. Nationwide
Termination Date
Sep 17, 2022
Product Description
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
Batch or Lot Expiration Information
Lot# : C040591, Exp 4/21
Affected Packages Involved in this Recall
47593-490-82Product
47593-490-87Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
