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Class II: temporary or reversible health riskTerminated

Midlab Corsair Personal Care 99X Instant Foam Hand Recall

Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0

Midlab Incorporated · Athens, TN

Risk level
Class II
Reported by FDA
Aug 31, 2022
Recall ID
D-1464-2022
Check your lot numberHow we source this data

Summary

Midlab recalled Corsair Personal Care 99X Instant Foam Hand starting Aug 8, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1464-2022 on Aug 31, 2022. Reason: CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride. Status: Terminated.

Why it was recalled

CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

Product description

Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028

Lot numbers, UPCs & expiration codes

Lot #: 06172022-1

Where it was sold

Naionwide within the United States

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-1464-2022
Classification
Class II
Status
Terminated
Recall initiated
Aug 8, 2022
FDA report date
Aug 31, 2022
Recall type
Voluntary: Firm initiated
Recalling firm
Midlab Incorporated

Original FDA data

Every field from FDA enforcement report D-1464-2022, exactly as published.

Show all FDA fields
City
Athens
State
TN
Status
Terminated
Country
United States
Event ID
90756
Address
140 Private Brand Way
Code information
Lot #: 06172022-1
Postal code
37303-1401
Report date
Aug 31, 2022
Product type
Drugs
Recall number
D-1464-2022
Classification
Class II
Recalling firm
Midlab Incorporated
Termination date
Aug 15, 2023
Reason for recall
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028
Distribution pattern
Naionwide within the United States
Recall initiation date
Aug 8, 2022
Initial firm notification
Letter
Center classification date
Aug 25, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1464-2022, published Aug 31, 2022. 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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