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Class II: temporary or reversible health riskTerminated

S.C. Johnson Professional deb stoko Recall

deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0

S.C. Johnson Professional · Charlotte, NC

Risk level
Class II
Reported by FDA
Nov 14, 2018
Recall ID
D-0220-2019
Check your lot numberHow we source this data

Summary

S.C. Johnson Professional recalled deb stoko starting Oct 26, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0220-2019 on Nov 14, 2018. Reason: CGMP Deviations: Product was released to market prior to microbiological testing. Status: Terminated.

Why it was recalled

CGMP Deviations: Product was released to market prior to microbiological testing.

Product description

deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.

Lot numbers, UPCs & expiration codes

Lot 9131

Where it was sold

NC

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-0220-2019
Classification
Class II
Status
Terminated
Recall initiated
Oct 26, 2018
FDA report date
Nov 14, 2018
Quantity
869 cases
Recall type
Voluntary: Firm initiated
Recalling firm
S.C. Johnson Professional

Original FDA data

Every field from FDA enforcement report D-0220-2019, exactly as published.

Show all FDA fields
City
Charlotte
State
NC
Status
Terminated
Country
United States
Event ID
81453
Address
2815 Coliseum Centre Dr Ste 600
Code information
Lot 9131
Postal code
28217-0144
Report date
Nov 14, 2018
Product type
Drugs
Recall number
D-0220-2019
Classification
Class II
Recalling firm
S.C. Johnson Professional
Product quantity
869 cases
Termination date
Sep 8, 2020
Reason for recall
CGMP Deviations: Product was released to market prior to microbiological testing.
Voluntary / mandated
Voluntary: Firm initiated
Product description
deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.
Distribution pattern
NC
Recall initiation date
Oct 26, 2018
Initial firm notification
Telephone
Center classification date
Nov 6, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0220-2019, published Nov 14, 2018. 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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