2 fully baked pizza shells packed in plastic bag with labeling reading recall
Recalled by Cowden's Lycoming Bakery · S. Williamsport, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lycoming Bakery Pizza Shells contain whey. Whey was not identified as a milk allergen.
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
2 fully baked pizza shells packed in plastic bag with labeling reading: Cowden's Lycoming Bakery 220 Curtain St, South Williamsport, PA; 2 Pizza Shells Net Wt. 20 oz. Ingredients: ***Flour (Hard Spring wheat flour), water, shortening (partially hydrogenated soybean and cottonseed oil), reddisponge (whey, corn flour, monocalcium phosphate, L-cysteine hydrochloride, potassium bromate), yeast***
Quantity: 123 units
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.
UPC 03410 00013 no expiration or pull by dates
Where it was sold
Pennsylvania
FDA's distribution note: PA in/around South Williamsport area.
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. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
- Cowden's Lycoming Bakery
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 2, 2015
- In FDA report of
- Aug 12, 2015
- Terminated
- Aug 14, 2015
- FDA recall number
- F-2933-2015 · event 71686
- Official record
- FDA enforcement report search