CPSC
Branch Recalls Ergonomic Chairs Due to Fall Hazard
The backrests of the chairs can detach, posing a fall hazard to consumers.
FDAClass II
Product is Potato Sourdough Bread and sold under three following names: Potato Market Loa… Recalled: Foreign object: May contain metal pieces
Product is Potato Sourdough Bread and sold under three… was recalled on August 12, 2026 in cooperation with the U.S. Food and Drug Administration because foreign object: May contain metal pieces.
Is my unit affected?
Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz. UPC 733163001576, product is sold at grocery stores with paper packaging. Label declares Potato Grand Central Rustic Breads ***A hearty sourdough loaf made with house-roasted potatoes. ***" Potato Table Loaf 20oz. No UPC. Product is sold direct to consumer at Grand Central Cafe stores and wholesalers without paper packaging. Mini Potato Loaf 12oz. No UPC. Product is sold at grocery stores and wholesalers without paper packaging.
Model, lot & date codes to check
No codes. Product was sold on 8/10/26.
Units affected: Potato Market Loaf 20oz = 288 units; Potato Table Loaf 20oz = 58 units; Mini Potato Loaf 12oz = 171 units
Where it was sold: Distributed in WA only.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
What's the hazard?
Foreign object: May contain metal pieces
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Your remedy & how to claim it
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc.
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Official recall notice
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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