CLASS I Food recall · Reported 23 May 2018 · FDA Enforcement Report

Golf Organic Dark Cocoa Raspberry bar recalled by eBars

eBars is recalling Golf Organic Dark Cocoa Raspberry bar, distributed in 40 states. The recall was initiated on 5 Feb 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots and date codes
Quantity recalled4,284/1.6 oz 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-1448-2018
FDA event ID
79138
Recalling firm
eBars, Franklin, TN
Brand
Golf
Classification
Class I
Status
Terminated
Recall initiated
5 Feb 2018
FDA classified
15 May 2018
Reported
23 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Peanuts
Product category
Chocolate

Timeline

5 Feb 2018Recall initiated by company
15 May 2018Classified by FDA+99 days
23 May 2018Published in enforcement report+8 days

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

Reason for recall

The product test positive for peanut allergen which is not declared on the product label.

Product as listed by the FDA

GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00402 8

Where it was distributed

Product was shipped to the following states:AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KS, KY, LA, MN, MD, MI, MN, MS, MO, MT, NC, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA & WV.

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIllinoisIndianaKansasKentuckyLouisianaMarylandMichiganMinnesota

Questions about this recall

Is Golf Organic Dark Cocoa Raspberry bar recalled?

Yes. eBars recalled Golf Organic Dark Cocoa Raspberry bar on 5 Feb 2018. The recall is Class I and its status is Terminated. Recall number F-1448-2018.

Why was it recalled?

The product test positive for peanut allergen which is not declared on the product label.

Which lots are affected?

All lots and date codes

Where was it sold?

Product was shipped to the following states:AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KS, KY, LA, MN, MD, MI, MN, MS, MO, MT, NC, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA & WV.

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 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 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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