CLASS II Drug recall · Reported 31 Aug 2022 · FDA Enforcement Report
Corsair Personal Care 99X Instant Foam Hand Sanitizer recalled
Midlab is recalling Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%). The recall was initiated on 8 Aug 2022 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1464-2022
- FDA event ID
- 90756
- Recalling firm
- Midlab, Athens, TN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Aug 2022
- FDA classified
- 25 Aug 2022
- Reported
- 31 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Hand Sanitizer
Timeline
| 8 Aug 2022 | Recall initiated by company | |
| 25 Aug 2022 | Classified by FDA | +17 days |
| 31 Aug 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Product as listed by the FDA
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
Where it was distributed
Naionwide within the United States
Questions about this recall
Why was it recalled?
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Which lots are affected?
Lot #: 06172022-1
Where was it sold?
Naionwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 90756| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) recalled | Midlab | Manufacturing (CGMP) Deviations | TN |
More recalls from Midlab
All 8| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Maxim Assure Antibacterial, Chloroxylenol recalled | Midlab | Potency & Assay | Nationwide |
| Drug | CLASS II | Genuine Joe Antibacterial Lotion Soap , Chloroxylenol recalled | Midlab | Potency & Assay | Nationwide |
| Drug | CLASS II | Compliance Dishwashing Liquid & Antibacterial Soap recalled | Midlab | Potency & Assay | Nationwide |
| Drug | CLASS II | boardwalk Antibacterial Handsoap Refill, Chloroxylenol recalled | Midlab | Potency & Assay | Nationwide |
| Drug | CLASS II | Array Liquid Antiseptic Handwash, Chloroxylenol recalled | Midlab | Potency & Assay | Nationwide |