RecallRadar

FDA Drug recall D-1463-2022

Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b)…

On 2022-08-31 the FDA classified a Class II recall of Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b)… by Midlab, citing CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1463-2022
ClassificationClass II
Statusterminated
Initiated2022-08-08
Published2022-08-31
Last updated2026-09-13 11:52 UTC
CompanyMidlab
Distributionn/a

Product

Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303

Reason

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

Identifiers

upc761841025026
upc00761841025040
code_infoLot #: a) 03292022-1, 05092022-1, 02012022-1, 06172022-1, 12132021-1, 07272022-1, and b) 06252022-1

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1463-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.