DFA Dairy Brands Fluid, LLC Recall: 1% Low Fat Milk potentially contaminated with sanitizer
United States
TerminatedClass II
- Company
- DFA Dairy Brands Fluid, LLC
- Product
- Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper ha…
- Recall date
- March 10, 2023
- Terminated
- April 14, 2023
- Source
- FDA
Reason for recall
1% Low Fat Milk potentially contaminated with sanitizer
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper half pint cartons - 50 cartons per case, Keep Refrigerated | Not published in this source record | 547 cartons | Batch No: Mar 24 UPC: 04190007778 Manufacturer No: Grad A IMS # 47-118 Best By Mar 24 Time Stamp 0930 to 0933 |
Distribution
- Alabama
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0694-2023
- Event ID
- 91946
- Status
- Terminated
- Classification
- Class II
- Company
- DFA Dairy Brands Fluid, LLC
- Product description
- Purity Sweet Acidophilus 1% Lowfat Milk packaged in paper half pint cartons - 50 cartons per case, Keep Refrigerated
- Quantity
- 547 cartons
- Reason
- 1% Low Fat Milk potentially contaminated with sanitizer
- Recall initiation date
- March 10, 2023
- Report date
- April 12, 2023
- Classification date
- Not published in this source record
- Termination date
- April 14, 2023
- Distribution pattern
- Alabama
- UPC, lot, and code information
- Batch No: Mar 24 UPC: 04190007778 Manufacturer No: Grad A IMS # 47-118 Best By Mar 24 Time Stamp 0930 to 0933
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: DFA Dairy Brands Fluid, LLC
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.
