Class IITerminated · reported 2024-12-25

Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag

GRIFFITH FOODS LTD recalled this product and the FDA reported the enforcement action on 25 December 2024 as Class II. The recall was initiated by the firm. potential for pieces of metal in product

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: Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag
Reason for recall: potential for pieces of metal in product
Recalling firm: GRIFFITH FOODS LTD
Firm location: Alsip, Illinois, United States
Classification: Class II
Status: Terminated
Recall number: F-0308-2025
Quantity: 25,903.154 lbs. (total)
Distribution: IL, NY, NC, WI, TX, TN, GA
Initiated: 1 November 2024
Reported by FDA: 25 December 2024
Terminated: 7 March 2025
Firm notified by: Letter
Product codes: LOT 579324

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. 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 5 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 5 separate recalls, which almost every published figure does, overstates it by a factor of 5. All 5 of them are listed on this page.
The recall ran for 4 months, from 1 November 2024 to termination on 7 March 2025. 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 7 states, and the FDA published the enforcement report 8 weeks 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: Illinois, New York, North Carolina, Wisconsin, Texas, Tennessee, Georgia. 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

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.

Every product in this recall

The FDA opened 5 enforcement records for this one recall, one per product code. This page carries all of them; the 4 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 4 records of FDA event 95763
Reported	Product	Firm	Reason	Class
2024-12-25	Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 25293502, ADHESION BREADER EX, 50 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II

Other records from GRIFFITH FOODS LTD

The FDA opens one enforcement record per product code, so several of these are frequently one recall event.

Reported	Product	Firm	Reason	Class
2024-12-25	Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 25293502, ADHESION BREADER EX, 50 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II
2024-12-25	Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag	GRIFFITH FOODS LTD	potential for pieces of metal in product	Class II

All 5 records for GRIFFITH FOODS LTD

All 2024 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 access

Recall 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.