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Class III: unlikely to cause harmTerminated

Ecolab QUIK-CARE Aerosol Foam Hand Sanitizer Recall

QUIK-CARE Aerosol Foam Hand Sanitizer (62

Ecolab Inc · Saint Paul, MN

Risk level
Class III
Reported by FDA
Jun 26, 2019
Recall ID
D-1393-2019
Check your lot numberHow we source this data

Summary

Ecolab recalled QUIK-CARE Aerosol Foam Hand Sanitizer starting May 10, 2019. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1393-2019 on Jun 26, 2019. Reason: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material. Status: Terminated.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

Lot #: C040591, Exp 4/21

Where it was sold

U.S.A. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1393-2019
Classification
Class III
Status
Terminated
Recall initiated
May 10, 2019
FDA report date
Jun 26, 2019
Quantity
183 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Ecolab Inc

Original FDA data

Every field from FDA enforcement report D-1393-2019, exactly as published.

Show all FDA fields
City
Saint Paul
State
MN
Status
Terminated
Country
United States
Event ID
83114
Address
1 Ecolab Pl
Code information
Lot #: C040591, Exp 4/21
Postal code
55102-2739
Report date
Jun 26, 2019
Product type
Drugs
Recall number
D-1393-2019
Classification
Class III
Recalling firm
Ecolab Inc
Product quantity
183 cases
Termination date
Sep 17, 2022
Reason for recall
Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
U.S.A. Nationwide
Recall initiation date
May 10, 2019
Initial firm notification
Letter
Center classification date
Jun 18, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1393-2019, published Jun 26, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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