FDA Drug Recalls

Recalls / Class II

Class IID-1357-2022

Product

Stage 2-Ophardt Foaming Hand Sanitizer, Fragrance-Free, 1000 mL (33.9 fl. oz.) per bottle, Manufactured for 2XL Corporation, 2 Gateway Ct, Ste A, Bolingbrook, IL 60440

Affected lot / code info
Product Number 46101, Lots 722712-exp 07/22, 724755-exp 11/22, 725054-exp 12/22

Why it was recalled

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Recalling firm

Firm
Aire-Master of America Inc
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1821 N State Highway Cc, Nixa, Missouri 65714-8015

Distribution

Quantity
4,632 cartons
Distribution pattern
Florida, Illinois, Iowa, New Jersey

Timeline

Recall initiated
2022-07-15
FDA classified
2022-08-18
Posted by FDA
2022-08-24
Terminated
2023-02-19
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1357-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.