Summary
The FDA issued a Class I for ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US by Mead Johnson & Company. 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 bat.
Details
Source
Food Recall
External ID
F-0623-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
Lot/Code Info: Batch: ZL2HZF; SKU: 300871214415; lot:0670975; Expiry: 3/1/2024 Batch: ZL2HZZ; SKU: 300871214415; lot:0670979; Expiry: 3/1/2024
Quantity Affected: 147,230 cans
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.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-19
Company
Zeeland, MI
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mead Johnson & Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mead Johnson & Company have FDA actions?
This is the only FDA action we have on record for Mead Johnson & Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0623-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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