AIP Veggie Pizza; Small, Medium; Large; made to order pizzas; packaged in boxes for…
Wegmans Food Markets, Inc. recalled this product and the FDA reported the enforcement action on 2 September 2020 as Class III. The recall was initiated by the firm. Products are potentially contaminated with Listeria monocytogenes.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- AIP Veggie Pizza; Small, Medium; Large; made to order pizzas; packaged in boxes for takeout; refrigerate
- Reason for recall
- Products are potentially contaminated with Listeria monocytogenes.
- Recalling firm
- Wegmans Food Markets, Inc.
- Firm location
- Rochester, New York, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-1315-2020
- Quantity
- 2,688 total units sold
- Distribution
- VA, NJ, MD, PA, NC, NY
- Initiated
- 7 August 2020
- Reported by FDA
- 2 September 2020
- Terminated
- 31 August 2020
- Firm notified by
- Other
- Product codes
- Purchased from 8/5/2020 through 8/7/2020. Small - UPC: 23738600000 and Sell by 8/9/2020 Medium - UPC: 23740400000 and Sell by 8/9/2020 Large - UPC: 23741400000 and Sell by 8/9/2020
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 23 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 23 separate recalls, which almost every published figure does, overstates it by a factor of 23. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 23 of them.
- The recall ran for 3 weeks, from 7 August 2020 to termination on 31 August 2020. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 6 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of a prepared meal or sandwich run a median of 6 months, so this one was shorter than usual for its category. Prepared meals concentrate every other category's hazards into one package: they are assembled from many components, handled after any cook step, sold ready to eat, and carry an ingredient list long enough to lose an allergen in.
Named in the distribution pattern: Virginia, New Jersey, Maryland, Pennsylvania, North Carolina, New York. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Listeria monocytogenes
Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.
A preventive controls plan covers Listeria contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(3)
- Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
- 21 CFR 117.165(a)(3)
- Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under prepared meals and sandwiches. A product can sit in more than one.
Other prepared meals and sandwiches recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Wegmans Food Markets, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 150 other records name this firm.
All 151 records for Wegmans Food Markets, Inc.
All 2020 recalls · All FDA food recall data
21 CFR 117.135(c)(3) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.