CLASS II Food recall · Reported 2 Nov 2016 · FDA Enforcement Report

Wilton Red Airbrush Color recalled

Wilton Brands is recalling Wilton Red Airbrush Color, distributed nationwide in the US. The recall was initiated on 6 Sep 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: 701-2413; 2201-2578
Quantity recalled16,197 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0361-2017
FDA event ID
75097
Recalling firm
Wilton Brands, Woodridge, IL
Brand
Wilton
Classification
Class II
Status
Terminated
Recall initiated
6 Sep 2016
FDA classified
26 Oct 2016
Reported
2 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Mold
Product category
Other

Timeline

6 Sep 2016Recall initiated by company
26 Oct 2016Classified by FDA+50 days
2 Nov 2016Published in enforcement report+7 days

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

Reason for recall

Airbrush color has the potential to be contaminated with mold, yeast or bacteria.

Product as listed by the FDA

Wilton Red Airbrush Color, Net Wt 0.64 FL OZ (19 mL)

Where it was distributed

Nationwide in U.S. and Canada

Nationwide

Questions about this recall

Is Wilton Red Airbrush Color recalled?

Yes. Wilton Brands recalled Wilton Red Airbrush Color on 6 Sep 2016. The recall is Class II and its status is Terminated. Recall number F-0361-2017.

Why was it recalled?

Airbrush color has the potential to be contaminated with mold, yeast or bacteria.

Which lots are affected?

Lots: 701-2413; 2201-2578

Where was it sold?

Nationwide in U.S. and Canada

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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