Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA, WHO, and other public sources. It is an independent information service, not a medical provider, and not a substitute for professional medical advice or your local public health department's own guidance.
Please review the following before continuing:
Policy version 2026-07-21, effective July 21, 2026.
United States
OngoingClass II
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413 | 015000005962 | 258,474 cases | Product Number: 12212034 Batch Code/Best If Used By Date: - 5198565504 BB: 16 OCT 2026 - 5202565504 BB: 20 OCT 2026 - 5203565504 BB: 21 OCT 2026 - 5204565504 BB: 22 OCT 2026 - 5205565504 BB: 23 OCT 2026 - 5209565504 BB: 27 OCT 2026 - 5210565504 BB: 28 OCT 2026 - 5211565504 BB: 29 OCT 2026 - 5233565504 BB: 20 NOV 2026 - 5238565504 BB: 25 NOV 2026 - 5239565504 BB: 26 NOV 2026 - 5239565505 BB: 26 NOV 2026 - 5240565505 BB: 27 NOV 2026 - 5245565505 BB: 02 DEC 2026 - 5246565505 BB: 03 DEC 2026 - 5251565505 BB: 08 DEC 2026 - 5252565505 BB: 09 DEC 2026 - 5253565505 BB: 10 DEC 2026 - 5254565505 BB: 11 DEC 2026 - 5258565505 BB: 15 DEC 2026 - 5259565505 BB: 16 DEC 2026 |
Responsible company: Gerber Products Company dba Nestle Infant Nutrition
FDA Recall United States Terminated Historical recordClass III
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
