Class ITerminated in FDA datasetRecall initiated Feb 5, 2018

WOMAN ORGANIC DARK CHOCOLATE BERRY bar NET WT. 1.8 OZ (51g) Manufactured and

Recalling firm: eBars

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 12, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductWOMAN ORGANIC DARK CHOCOLATE BERRY bar NET WT. 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00418 9
Package size1.8 OZ
UPC855529004189

FDA code information

All lots and date codes

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

WOMAN ORGANIC DARK CHOCOLATE BERRY bar NET WT. 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00418 9

Extracted codes and context

TypeCode / valueContext
UPC8555290041891.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00418 9

Original FDA recall reason

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

Recall details

Recall number
F-1455-2018
Event ID
79138
FDA status
Terminated
Initiated
Feb 5, 2018
Reported
May 23, 2018
Classified
May 15, 2018
Terminated
Oct 12, 2018
Quantity
38,273/1.8oz bars
Location
Franklin, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

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.

FDA source record · F-1455-2018

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.