Data Foundry

Drug recalls 2017

Option Systems Antibacterial Foaming Hand Wash — Class II drug recall D-0002-2018

Terminated recall by Inopak Ltd, reported 2017-10-11, distributed nationwide. GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated

Recall numberD-0002-2018
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmInopak Ltd, Ringwood, NJ, United States
Recall initiated2017-08-23
Classified2017-10-04
Reported by FDA2017-10-11
Terminated2020-04-20
DistributedNationwide (US)
Reason classesmicrobial contamination, cgmp
Lot numbers6718, 6725, 6730, 6732, 6735, 6742, 6744, 6754, 6756, 6760, 6762, 6766, 6770, 6773, 6777, 6784, 6792, 6793, 6798, 6804, 6807, 6812, 6813, 6816, 6819, 6820, 6829, 6838, 6839, 6846, 6862, 6868, 6872, 6875, 6877, 6890, 6891, 6902, 6904, 6906 and 9 more

Product

Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and 1000 mL pouches, ALSO labeled as STYLE Antibacterial Hand Soap, Inopak Ltd Ringwood, NJ --- NDC 5031-431-02

Reason for recall

GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump

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-0002-2018. 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.