FDA recall, , Moderate risk
Tippy Toes Apple Pear Banana Baby Food
Tippy Toes apple pear banana baby food may be contaminated with patulin, which can cause health issues.
Summary by Recall Canary from the FDA notice
What happened
IF Holding II, LLC of Sanger, California began a recall of tippy toes apple pear banana 6 months & up baby food on February 5, 2026, due to potential contamination with patulin. The company announced the recall on February 13, 2026, and the FDA added it to the Enforcement Report on March 5, 2026. The product was distributed to U.S. consignees in Illinois. The recall involves 1,375 cases of the baby food, which is distributed by Topco Associates LLC of Elk Grove Village, Illinois.
The product is described as tippy toes apple pear banana 6 months & up baby food in 2-4OZ (113g) packs, with a net weight of 8 OZ (226g). The recall was prompted by elevated levels of patulin. The product is a product of the USA.
2 photos
What to do
If a code on your package is listed below:
- For further recall information and updates, consumers and retailers can call a dedicated toll-free number: 1-855-215-5730, Monday through Friday, 8 a.m. to 5 p.m. Eastern Standard Time.
- Consumers with the Product matching the “Best By” (expiration) date of July 17, 2026 should.
- Retailers should check inventory and shelves, and immediately remove the affected lot from sale or distribution and catalogue the recalled product.
Is yours affected?
Affected if its lot code, UPC and package code identifier are listed under that product.
A UPC is the number printed under a barcode.
Tippy Toes Apple Pear Banana
- UPC
- 036800
- 265783
- UPC
- 036800265783
- Lot code
- 07174
- Best By Date:
- “BB 07/17/2026”
- Package code identifier
- INIA0120
- Packaging format
- 2-pack plastic tubs, with product information sleeve
Recall details
- Company began the recall
- Sold in
U.S. Consignees: Illinois
- Company
- IF Holding II, LLCSanger, California
- Hazard
- Chemical contamination
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98337
- Recall number
- H-0544-2026
- Quantity recalled
- 1375 cases
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
