Mead Johnson & Company Recall: Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.
United States
TerminatedClass I
- Company
- Mead Johnson & Company
- Product
- ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
- Recall date
- February 19, 2023
- Terminated
- November 26, 2024
- Source
- FDA
Reason for recall
Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US | Not published in this source record | 147,230 cans | Batch: ZL2HZF; SKU: 300871214415; lot:0670975; Expiry: 3/1/2024 Batch: ZL2HZZ; SKU: 300871214415; lot:0670979; Expiry: 3/1/2024 |
Distribution
- AK
- AL
- AR
- AZ
- CA
- CO
- CT
- FL
- GA
- HI
- IA
- IL
- IN
- KY
- LA
- MA
- ME
- MI
- MN
- MO
- MS
- NC
- NH
- NJ
- NV
- NY
- OH
- OK
- OR
- PA
- RI
- SC
- TN
- TX
- UT
- VA
- WA
- WI
- Puerto Rico. Foreign: Bangkok
- Thailand and Guam.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0623-2023
- Event ID
- 91743
- Status
- Terminated
- Classification
- Class I
- Company
- Mead Johnson & Company
- Product description
- ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
- Quantity
- 147,230 cans
- Reason
- Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.
- Recall initiation date
- February 19, 2023
- Report date
- March 22, 2023
- Classification date
- Not published in this source record
- Termination date
- November 26, 2024
- Distribution pattern
- AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, Puerto Rico. Foreign: Bangkok, Thailand and Guam.
- UPC, lot, and code information
- Batch: ZL2HZF; SKU: 300871214415; lot:0670975; Expiry: 3/1/2024 Batch: ZL2HZZ; SKU: 300871214415; lot:0670979; Expiry: 3/1/2024
- 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
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 |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Hawaii | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 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 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?
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