CLASS I Drug recall · Reported 12 Aug 2020 · FDA Enforcement Report

Lemon Blossom Hand Sanitizer (benzalkonium chloride recalled

Spartan Chemical is recalling Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For, distributed nationwide in the US. The recall was initiated on 1 Jul 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesa) 42.27 oz cartridge: 518491, 518492, 518498, 518499, 518500, 520057, 520058, 520060, 520061; b) 1 gallon container: 520032, Exp. 06/30/2022.
Quantity recalleda) 60,796 cartridges, b) 420 gallon containers

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1503-2020
FDA event ID
85978
Recalling firm
Spartan Chemical, Maumee, OH
Classification
Class I
Status
Terminated
Recall initiated
1 Jul 2020
FDA classified
14 Aug 2020
Reported
12 Aug 2020
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Sterility
Drug class
Hand Sanitizer

Timeline

1 Jul 2020Recall initiated by company
12 Aug 2020Published in enforcement report+42 days
14 Aug 2020Classified by FDA+2 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Microbial contamination of non-sterile products: positive microbial contamination in product.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For Institutional and Industrial Use Only, a) foamyiQ 42.27 oz/1250 mL cartridge, UPC code: 7 53727 26454 4; b) Lite 'n Foamy 1 gallon/3.79 L container UPC code: 7 53727 26113 0, Spartan Chemical Company, Inc., 1110 Spartan Drive, Maumee, OH 43537 USA.

Where it was distributed

Nationwide USA, Panama, St. Maarten

Nationwide

Questions about this recall

Why was it recalled?

Microbial contamination of non-sterile products: positive microbial contamination in product.

Which lots are affected?

a) 42.27 oz cartridge: 518491, 518492, 518498, 518499, 518500, 520057, 520058, 520060, 520061; b) 1 gallon container: 520032, Exp. 06/30/2022.

Where was it sold?

Nationwide USA, Panama, St. Maarten

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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