Data Foundry

Drug recalls 2021

AmericanScreening HAND SANITIZER — Class I drug recall D-0266-2022

Completed recall by American Screening LLC, reported 2021-12-15, distributed nationwide. Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

Recall numberD-0266-2022
Product typeDrug
ClassificationClass I
StatusCompleted
Voluntary or mandatedVoluntary
Recalling firmAmerican Screening LLC, Shreveport, LA, United States
Recall initiated2021-11-19
Classified2021-12-06
Reported by FDA2021-12-15
DistributedNationwide (US)
Quantity153,336 bottles
Reason classeslabeling
UPC / GTIN / UDI-DI00840050515792

Product

AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2

Reason for recall

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0266-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.