Morrison's Corn Kits Prepares Cornbread Mix NET WT 6 OZ (170g) packed in paper box
C. H. Guenther & Son, Inc.dba Morrison Milling recalled this product and the FDA reported the enforcement action on 20 April 2016 as Class III. The recall was initiated by the firm. May contain small metal fragments from wire mesh sifter.
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
- Morrison's Corn Kits Prepares Cornbread Mix NET WT 6 OZ (170g) packed in paper box
- Reason for recall
- May contain small metal fragments from wire mesh sifter.
- Recalling firm
- C. H. Guenther & Son, Inc.dba Morrison Milling
- Firm location
- Denton, Texas, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-0839-2016
- Quantity
- 278,374 cases
- Distribution
- Nationwide throughout the US
- Initiated
- 7 December 2015
- Reported by FDA
- 20 April 2016
- Terminated
- 2 August 2016
- Firm notified by
- Letter
- Product codes
- All lots
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 81 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 81 separate recalls, which almost every published figure does, overstates it by a factor of 81. 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 81 of them.
- The recall ran for 8 months, from 7 December 2015 to termination on 2 August 2016. 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 FDA published the enforcement report 4 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.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material 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 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 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.
Other records from C. H. Guenther & Son, Inc.dba Morrison Milling
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 81 other records name this firm.
All 82 records for C. H. Guenther & Son, Inc.dba Morrison Milling
All 2016 recalls · All FDA food recall data
21 CFR 117.40 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.