FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 25293502, ADHESION BREADER EX, 50 lb. bag
- Published
- December 25, 2024
- Distribution
- Multiple states
GRIFFITH FOODS LTD Recall: potential for pieces of metal in product
United States
TerminatedClass II
- Company
- GRIFFITH FOODS LTD
- Product
- Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.1…
- Recall date
- November 1, 2024
- Terminated
- March 7, 2025
- Source
- FDA
Reason for recall
potential for pieces of metal in product
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag | Not published in this source record | 25,903.154 lbs. (total) | LOT 579324 |
Distribution
- IL
- NY
- NC
- WI
- TX
- TN
- GA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0308-2025
- Event ID
- 95763
- Status
- Terminated
- Classification
- Class II
- Company
- GRIFFITH FOODS LTD
- Product description
- Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag
- Quantity
- 25,903.154 lbs. (total)
- Reason
- potential for pieces of metal in product
- Recall initiation date
- November 1, 2024
- Report date
- December 25, 2024
- Classification date
- Not published in this source record
- Termination date
- March 7, 2025
- Distribution pattern
- IL, NY, NC, WI, TX, TN, GA
- UPC, lot, and code information
- LOT 579324
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 95763 with 4 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag
- Published
- December 25, 2024
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. ba…
- Published
- December 25, 2024
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag
- Published
- December 25, 2024
- Distribution
- Multiple states
Responsible company: GRIFFITH FOODS LTD
Other recalls from GRIFFITH FOODS LTD
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 25293502, ADHESION BREADER EX, 50 lb. bag
- Published
- December 25, 2024
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag
- Published
- December 25, 2024
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
GRIFFITH FOODS LTD
- Product
- Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. ba…
- Published
- December 25, 2024
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Illinois | 1 |
| New York | 1 |
| North Carolina | 1 |
| Wisconsin | 1 |
| Texas | 1 |
| Tennessee | 1 |
| Georgia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
