Check the Batch
Class IIITerminated in FDA datasetRecall initiated Aug 7, 2017

Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g)…

Recalling firm: Mary's Gone Crackers, Inc.

Why it was recalled

Recall of crackers due to pieces of blue grade plastic liner found inside the packaged cracker product.

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: Jan 2, 2018.

Check your package

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

ProductMary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole grain brown rice, whole grain quinoa, brown flax seeds, brown sesame seeds, filtered water, sea salt, wheat free tamari (water, whole soybeans, salt, vinegar). Contains: Soy. Unit UPC: 8 97580 00010 6; Case UPC: 8 97580 00030 4;
Package size6.5 oz
UPC897580000106, 897580000304

FDA code information

Lot Code: CK5572

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

Full FDA record and distribution details

Original product description

Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole grain brown rice, whole grain quinoa, brown flax seeds, brown sesame seeds, filtered water, sea salt, wheat free tamari (water, whole soybeans, salt, vinegar). Contains: Soy. Unit UPC: 8 97580 00010 6; Case UPC: 8 97580 00030 4;

Extracted codes and context

TypeCode / valueContext
UPC897580000106ree tamari (water, whole soybeans, salt, vinegar). Contains: Soy. Unit UPC: 8 97580 00010 6; Case UPC: 8 97580 00030 4;
UPC897580000304beans, salt, vinegar). Contains: Soy. Unit UPC: 8 97580 00010 6; Case UPC: 8 97580 00030 4;
lotCK5572Lot Code: CK5572

Original FDA recall reason

Recall of crackers due to pieces of blue grade plastic liner found inside the packaged cracker product.

Recall details

Recall number
F-3484-2107
Event ID
77909
FDA status
Terminated
Initiated
Aug 7, 2017
Reported
Sep 6, 2017
Classified
Aug 31, 2017
Terminated
Jan 2, 2018
Quantity
1,988 cases (12 x 6.5 oz. boxe per case).
Location
Gridley, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

To distributors in NC, CA, NY, IA, PA, CT, TX, NJ, KS, KY. IL:. CO 7 Distributors at multiple addresses.

FDA source record · F-3484-2107

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

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