Produce Packaging, Inc. Burger, Asian Veg. 4/10 OZ
Produce Packaging Inc recalled this product and the FDA reported the enforcement action on 6 March 2019 as Class I. The recall was initiated by the firm. Firm received notification from supplier of potential for contamination with E.coli.
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
- Produce Packaging, Inc. Burger, Asian Veg. 4/10 OZ
- Reason for recall
- Firm received notification from supplier of potential for contamination with E.coli.
- Recalling firm
- Produce Packaging Inc
- Firm location
- Cleveland, Ohio, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1096-2019
- Quantity
- 1
- Distribution
- OH, MI, NY, TX
- Initiated
- 18 December 2018
- Reported by FDA
- 6 March 2019
- Terminated
- 17 September 2019
- Firm notified by
- Product codes
- X0286568 15DEC18
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 22 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 22 separate recalls, which almost every published figure does, overstates it by a factor of 22. 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 22 of them.
- The recall ran for 9 months, from 18 December 2018 to termination on 17 September 2019. 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 4 states, and the FDA published the enforcement report 3 months after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Ohio, Michigan, New York, Texas. 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
E. coli
Shiga toxin-producing E. coli recalls concentrate in foods eaten raw or lightly cooked, where no step in the process is hot enough or long enough to be a kill step.
A preventive controls plan covers E. coli 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)(1)
- Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
- 21 CFR 120
- Juice HACCP: the hazard analysis and critical control point system required for juice processors, including a treatment achieving a 5-log pathogen reduction.
Other records from Produce Packaging Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 24 other records name this firm.
All 25 records for Produce Packaging Inc
All 2019 recalls · All FDA food recall data
21 CFR 117.135(c)(1) 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.