Mead Johnson & Company LLC Recall: Product has the potential to be contaminated with Cronobacter sakazakii.
United States
TerminatedClass I
- Company
- Mead Johnson & Company LLC
- Product
- Enfamil Nutramigen Hypoallergenic Infant Formula Powder with…
- Recall date
- December 30, 2023
- Terminated
- August 13, 2025
- Source
- FDA
Reason for recall
Product has the potential to be contaminated with Cronobacter sakazakii.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 or 300871239456 and Use By Date of "1 Jan 2025". | Not published in this source record | 1,396,438 cans | ZL3FHG (12.6 oz cans) ZL3FMH (12.6 oz cans) ZL3FPE (12.6 oz cans) ZL3FQD (12.6 oz cans) ZL3FRW (19.8 oz cans) ZL3FXJ (12.6 oz cans) |
Distribution
- Retail stores and medical facilities nationwide and outside the U.S.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0809-2024
- Event ID
- 93718
- Status
- Terminated
- Classification
- Class I
- Company
- Mead Johnson & Company LLC
- Product description
- Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 or 300871239456 and Use By Date of "1 Jan 2025".
- Quantity
- 1,396,438 cans
- Reason
- Product has the potential to be contaminated with Cronobacter sakazakii.
- Recall initiation date
- December 30, 2023
- Report date
- January 24, 2024
- Classification date
- Not published in this source record
- Termination date
- August 13, 2025
- Distribution pattern
- Retail stores and medical facilities nationwide and outside the U.S.
- UPC, lot, and code information
- ZL3FHG (12.6 oz cans) ZL3FMH (12.6 oz cans) ZL3FPE (12.6 oz cans) ZL3FQD (12.6 oz cans) ZL3FRW (19.8 oz cans) ZL3FXJ (12.6 oz cans)
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Mead Johnson & Company LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
