Italian White Bread Dough Sticks
Reason Aryzta LLC is recalling multiple lots of bread dough following a supplier's recall of a yeast ingredient due to potential contamination with metal fragments.
Italian White Bread Dough Sticks recall
Recalled by Aryzta North America · Cayce, SC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Aryzta LLC is recalling multiple lots of bread dough following a supplier's recall of a yeast ingredient due to potential contamination with metal fragments.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Italian White Bread Dough Sticks
Quantity: 1872 cases (26.25 lbs of dough per case) (70/6oz. sticks per case)
Food: Bread & bakery
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Item # : 24339 Batch #s: 8CA002A2 and 7CA363C1
Where it was sold
Florida Puerto Rico
FDA's distribution note: Subway distribution warehouses in Florida and Puerto Rico - Items # 24339 and 24559 only. Item 24558 as identified on the Attachment B record was never shipped form the manufacturer's warehouse.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Aryzta North America
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 10, 2018
- In FDA report of
- Feb 28, 2018
- Terminated
- Oct 1, 2021
- FDA recall number
- F-0826-2018 · event 79003
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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