Son of Italy
Reason K.B. Pizza, Inc. has initiated a recall of Son of Italy Cheese Kit, Son of Italy Pepperoni Kit, 39 oz./2 pizzas per kit, Vacuum packed, 6 kits per case. Use by date of 12-5-18 on each kit and case, because the pizza…
Son of Italy Pepperoni Pizza Kit recall
Recalled by K.B. Pizza, Inc. · Franklin, PA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
K.B. Pizza, Inc. has initiated a recall of Son of Italy Cheese Kit, Son of Italy Pepperoni Kit, 39 oz./2 pizzas per kit, Vacuum packed, 6 kits per case. Use by date of 12-5-18 on each kit and case, because the pizza kits were left at room temperature for 24 hours, with cheese packs in the kits.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Son of Italy Pepperoni Pizza Kit ,39 oz./2 pizzas per kit, Net Wt. 15.5 lbs. 6 pizza kits per case
Quantity: 144 cases
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.
Use By 12-5-18
Where it was sold
Maryland
FDA's distribution note: All cases were distributed to the following location: Pastores Inc. 6101 E. Lombard St Baltimore, MD 21224
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- K.B. Pizza, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 3, 2018
- In FDA report of
- Oct 24, 2018
- Terminated
- Jun 18, 2019
- FDA recall number
- F-0036-2019 · event 81267
- 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.