CLASS II Food recall · Reported 20 May 2015 · FDA Enforcement Report

KT's Energy Bars recalled by Taylor Catering

Taylor Catering is recalling KT's Energy Bars, distributed in Oregon. The recall was initiated on 2 Apr 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesno codes
Quantity recalled180 bars

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-2200-2015
FDA event ID
70928
Recalling firm
Taylor Catering, Bend, OR
Brand
KT's
Classification
Class II
Status
Terminated
Recall initiated
2 Apr 2015
FDA classified
8 May 2015
Reported
20 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Soy
Product category
Granola Bars

Timeline

2 Apr 2015Recall initiated by company
8 May 2015Classified by FDA+36 days
20 May 2015Published in enforcement report+12 days

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

Reason for recall

KT's Energy Bars are recalled due to undeclared soy lecithin.

Product as listed by the FDA

KT's Energy Bars, net weight per bar is 2.9 oz (82.21 g).

Where it was distributed

distributed in Oregon

Oregon

Questions about this recall

Is KT's Energy Bars recalled?

Yes. Taylor Catering recalled KT's Energy Bars on 2 Apr 2015. The recall is Class II and its status is Terminated. Recall number F-2200-2015.

Why was it recalled?

KT's Energy Bars are recalled due to undeclared soy lecithin.

Which lots are affected?

no codes

Where was it sold?

distributed in Oregon

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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