Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans
Reason Product has the potential to be contaminated with Cronobacter sakazakii.
Enfamil Prosobee Pwd recall
Recalled by Mead Johnson & Company · Zeeland, MI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
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.
Pathogen: Cronobacter
A bacterium of particular concern in powdered infant formula.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
Quantity: 147,230 cans
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch: ZL2HZF; SKU: 300871214415; lot:0670975; Expiry: 3/1/2024 Batch: ZL2HZZ; SKU: 300871214415; lot:0670979; Expiry: 3/1/2024
Where it was sold
Alaska Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Hawaii Iowa Illinois Indiana Kentucky Louisiana Massachusetts Maine Michigan Minnesota Missouri Mississippi North Carolina New Hampshire New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina Tennessee Texas Utah Virginia Washington Wisconsin
FDA's distribution note: 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.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Mead Johnson & Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 19, 2023
- In FDA report of
- Mar 22, 2023
- Terminated
- Nov 26, 2024
- FDA recall number
- F-0623-2023 · event 91743
- Official record
- FDA enforcement report search