Hand sanitizer recalled for use of expired active ingredient
Corsair Personal Care 99X Instant Foam Hand Sanitizer is being recalled due to a manufacturing violation: it was made using expired benzalkonium chloride. Consumers should stop using the affected product.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving a manufacturing deviation with expired active ingredient. The source reports no illnesses or injuries. Per the severity rubric, a risk-of-harm product with no reported injury scores 3 (High). The expired active ingredient undermines product performance, but without reported harm, the severity does not exceed High.
Plain-English summary
Midlab Incorporated is recalling Corsair Personal Care 99X Instant Foam Hand Sanitizer (0.1% benzalkonium chloride) in 128 fl. oz. bottles distributed nationwide. The product was manufactured using an expired benzalkonium chloride, which violates Current Good Manufacturing Practices (CGMP). The affected product bears lot number 06172022-1.
The use of expired active ingredient means the product may not provide the intended sanitizing performance. Consumers who have purchased this product should stop using it and dispose of it safely.
No illnesses or injuries have been reported at this time. For more information, consumers may contact Midlab Incorporated or the FDA.
The recalled product
- Product
- 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
- Manufacturer
- Midlab Incorporated
- Category
- Drug — Hand Sanitizer
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 06172022-1
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Midlab Incorporated under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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