DiGiorno pizzeria bianca/white pizza
Reason Plastic contamination. Four pizzas with specific production codes, are being recalled because they may contain fragments of clear plastic
california Pizza Kitchen crispy thin crust recall
Recalled by Nestle USA, Inc - Northbrook Pizza Head Office · Northbrook, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Plastic contamination. Four pizzas with specific production codes, are being recalled because they may contain fragments of clear plastic
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
california Pizza Kitchen crispy thin crust, White, Crispy thin crust pizza topped with garlic creme fraiche sauce, spinach, garlic, mozzarella,cheeses, parmesan, asiago and romano cheeses. Net Wt.12.8 OZ (363 g), UPC 71921-98745
Quantity: 16,163 cases (14 pizzas/case)
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.
Production codes: 3062525951, 3062525952. and 3063525951
Where it was sold
Nationwide.
FDA's distribution note: US nationwide distribution only. NO OUS.
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
- Nestle USA, Inc - Northbrook Pizza Head Office
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2013
- In FDA report of
- Jun 12, 2013
- Terminated
- Nov 19, 2013
- FDA recall number
- F1467-2013 · event 65106
- 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.