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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Maxim and Corsair Instant Foam Hand Sanitizers Recalled for Expired Ingredient

Agency Publication Date: August 25, 2022
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Summary

Midlab Incorporated is recalling Maxim and Corsair Personal Care 99X Instant Foam Hand Sanitizers containing 0.1% benzalkonium chloride (the active ingredient). Approximately 892 one-gallon bottles and one 55-gallon drum are affected because they were manufactured using an expired batch of benzalkonium chloride. While no incidents or injuries have been reported, using sanitizer with an expired active ingredient may not provide the intended protection against germs.

Risk

The use of an expired active ingredient may result in the hand sanitizer being less effective than expected at killing germs, potentially increasing the risk of infection. No injuries have been reported in connection with this recall.

What You Should Do

  1. This recall affects Maxim Instant Foam Hand Sanitizer and Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) sold in 1-gallon bottles and 55-gallon drums.
  2. Identify the affected Maxim product by checking for lot numbers 03292022-1, 05092022-1, 02012022-1, 06172022-1, 12132021-1, 07272022-1, or 06252022-1 and UPC codes 761841025026 or 00761841025040.
  3. Identify the affected Corsair Personal Care 99X product by checking for lot number 06172022-1 on 128 fl. oz. (1 gallon) bottles.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Midlab Incorporated for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)
Variants: 1 U.S. Gallon (3.78 Liters) drums, 55 U.S. Gallon drums (208 Liters)
UPC Codes:
761841025026
00761841025040
Lot Numbers:
03292022-1
05092022-1
02012022-1
06172022-1
12132021-1
07272022-1
06252022-1

Manufactured by Midlab 140 Private Brand Way, Athens, TN 37303

Product: Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)
Variants: 128 Fl. Oz. (1 Gal.) 3.78 liters bottles
Lot Numbers:
06172022-1

Distributed by Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90756
Status: Resolved
Manufacturer: Midlab Incorporated
Sold By: Southern Products & Services, Inc.; Midlab Incorporated
Manufactured In: United States
Units Affected: 892 gallons and one 55-gallon drum
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.