FDA recall record
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 26, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
Code information listed by FDA
Batch: ZL2HZF; SKU: 300871214415; lot:0670975; Expiry: 3/1/2024 Batch: ZL2HZZ; SKU: 300871214415; lot:0670979; Expiry: 3/1/2024
Distribution and firm information
Recalling firm listed by FDA: Mead Johnson & Company
Firm location listed by FDA: Zeeland, MI, United States
Distribution reported by FDA: 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.
Product quantity listed by FDA: 147,230 cans
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.