FDA Recall United States Ongoing2026 recordClass II
Gerber Products Company dba Nestle Infant Nutrition
- Product
- Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged…
- Published
- March 4, 2026
- Distribution
- Nationwide
Gerber Products Company dba Nestle Infant Nutrition Recall: Beetles were found in the pea ingredient used in the side compartment of the tray.
United States
TerminatedClass III
- Company
- Gerber Products Company dba Nestle Infant Nutrition
- Product
- GERBER Macaroni and Cheese with a side of peas and carrots,…
- Recall date
- November 18, 2021
- Terminated
- February 14, 2022
- Source
- FDA
Reason for recall
Beetles were found in the pea ingredient used in the side compartment of the tray.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| GERBER Macaroni and Cheese with a side of peas and carrots, 6.6 oz. (187 g) drained weight 5.3 oz. (150 g), 8 units per case. | Not published in this source record | 4,278 cases released | 21775185XX Best By 04Oct2022 |
Distribution
- The product was distributed to the following states: DE
- ME
- VA
- PA
- CT
- NY
- MI
- TX
- WI
- OH
- AL
- IA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0271-2022
- Event ID
- 89087
- Status
- Terminated
- Classification
- Class III
- Company
- Gerber Products Company dba Nestle Infant Nutrition
- Product description
- GERBER Macaroni and Cheese with a side of peas and carrots, 6.6 oz. (187 g) drained weight 5.3 oz. (150 g), 8 units per case.
- Quantity
- 4,278 cases released
- Reason
- Beetles were found in the pea ingredient used in the side compartment of the tray.
- Recall initiation date
- November 18, 2021
- Report date
- December 15, 2021
- Classification date
- Not published in this source record
- Termination date
- February 14, 2022
- Distribution pattern
- The product was distributed to the following states: DE,ME,VA,PA,CT,NY,MI,TX,WI,OH,AL ,IA
- UPC, lot, and code information
- 21775185XX Best By 04Oct2022
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Gerber Products Company dba Nestle Infant Nutrition
Other recalls from Gerber Products Company dba Nestle Infant Nutrition
FDA Recall United States TerminatedTerminated: June 18, 2020Historical recordClass II
Gerber Products Company dba Nestle Infant Nutrition
- Product
- M&M's Everyday Cookie Dough (14oz), UPC 050000417353
- Published
- January 15, 2020
- Distribution
- All consignees are in the US
FDA Recall United States TerminatedTerminated: June 18, 2020Historical recordClass II
Gerber Products Company dba Nestle Infant Nutrition
- Product
- M&M's Holiday Cookie Dough (14 oz), UPC 050000881697
- Published
- January 15, 2020
- Distribution
- All consignees are in the US
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Delaware | 1 |
| Maine | 1 |
| Virginia | 1 |
| Pennsylvania | 1 |
| Connecticut | 1 |
| New York | 1 |
| Michigan | 1 |
| Texas | 1 |
| Wisconsin | 1 |
| Ohio | 1 |
| Alabama | 1 |
| Iowa | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
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.
Where can I find more official information?
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.
