Corsair Personal Care 99X Instant Foam Hand Sanitizer recall: CGMP Deviations
Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products &…
Why was Corsair Personal Care 99X Instant Foam Hand Sanitizer recalled?
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 06172022-1
- Product
- Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products &…
- Recalling firm
- Midlab Incorporated
- Distribution
- Naionwide within the United States
- Recall date
- August 31, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)