Similac Probiotic Tri-Blend
Reason Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive
Zone Perfect Fudge Graham bar recall
Recalled by Abbott Laboratories · Columbus, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Potential of foreign material (hard plastic) within product
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
Quantity: 646,668 bars
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.
Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138
Where it was sold
Alabama Arizona California Colorado Connecticut Florida Georgia Iowa Idaho Illinois Indiana Kansas Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri North Carolina Nebraska New Jersey Nevada New York Ohio Pennsylvania South Carolina South Dakota Tennessee Texas Utah Virginia Washington Wisconsin West Virginia
FDA's distribution note: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NV, NY, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Abbott Laboratories
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 28, 2023
- In FDA report of
- Apr 19, 2023
- Terminated
- Dec 14, 2023
- FDA recall number
- F-0698-2023 · event 92015
- Official record
- FDA enforcement report search
Other recalls by Abbott Laboratories
Similac Water Sterilized
Reason Compromised seal integrity which could lead to spoilage
Similac Stage 1 (Export Dominican Republic)
Reason Compromised seal integrity which could lead to spoilage
Similac Stage 1 (Export Colombia)
Reason Compromised seal integrity which could lead to spoilage