FDAClass IIJune 20, 2018

Option Systems Antibacterial Foaming Hand Wash with .3% recall: Sterility Concern

Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ

Why was Option Systems Antibacterial Foaming Hand Wash with .3% recalled?

Microbial contamination of NonSterile Product; FDA analysis returned out of specification results for total aerobic microbial counts

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

7302 01 039, 7302 03 039, 7302 01 040 and 7302 01 043

Product
Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ
Recalling firm
Inopak Ltd
Quantity
1345 cases
Distribution
Nationwide
Recall date
June 20, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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