CLASS II Food recall · Reported 29 Nov 2017 · FDA Enforcement Report

Wild Yeast Sourdough recalled by Arise Gluten Free Bakery

Arise Gluten Free Bakery is recalling Wild Yeast Sourdough, distributed in California. The recall was initiated on 13 Nov 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codeslot 1310187 exp. 10/06/2018
Quantity recalled73 loaves

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-0345-2018
FDA event ID
78548
Recalling firm
Arise Gluten Free Bakery, Arcata, CA
Classification
Class II
Status
Terminated
Recall initiated
13 Nov 2017
FDA classified
17 Nov 2017
Reported
29 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Bread

Timeline

13 Nov 2017Recall initiated by company
17 Nov 2017Classified by FDA+4 days
29 Nov 2017Published 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

Firm received a complaint from a customer reporting that small shards of glass were found on the top of a slice of bread.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Arise Gluten Free Bakery Wild Yeast Sourdough; NET WEIGHT 24 OZ (680 grams) UPC 095225600005

Where it was distributed

one distributor in CA

California

Questions about this recall

Why was it recalled?

Firm received a complaint from a customer reporting that small shards of glass were found on the top of a slice of bread.

Which lots are affected?

lot 1310187 exp. 10/06/2018

Where was it sold?

one distributor in CA

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 78548

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