FDA Drug recall D-0864-2018
Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ
- FDA Drug
- Class II
- terminated
- Published 2018-06-20
On 2018-06-20 the FDA classified a Class II recall of Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ by Inopak, citing microbial contamination of NonSterile Product; FDA analysis returned out of specification results for total aerobic microbial counts.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0864-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-16 |
| Published | 2018-06-20 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Inopak |
| Distribution | US |
Product
Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ
Reason
Microbial contamination of NonSterile Product; FDA analysis returned out of specification results for total aerobic microbial counts
Identifiers
| code_info | 7302 01 039, 7302 03 039, 7302 01 040 and 7302 01 043 |
|---|
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-0864-2018%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.