ACTIVE RECALL — CLASS IIActive recallH-0518-2026/FDA enforcement

Gerber Arrowroot Biscuits, NET WT

What you need to know

Class II
  • What happened

    Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Plastic fragments can pose a choking risk or irritate and injure the digestive tract.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Active recall · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameGerber Products Company Dba Nestle Infant Nutrition
Recalling firmGerber Products Company Dba Nestle Infant NutritionArlington, VA, United States
UPC / barcodes
0 15000 00596 20 15000 93572 6
Lot / date codes
  • 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
Distribution area
Nationwide

Nationwide and Puerto Rico

United States, Puerto Rico

Quantity affected258, 474 cases
Recall initiationFDA report date: March 4, 2026
FDA recall numberH-0518-2026

Beyond the headline

The recall, in context

Gerber Products Company Dba Nestle Infant Nutrition initiated this food recall on January 26, 2026. The FDA enforcement report states: 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. The FDA report lists distribution as: Nationwide and Puerto Rico.

The FDA enforcement report describes the reason as: 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.

Gerber Arrowroot Biscuits, NET WT was made or distributed by Gerber Products Company Dba Nestle Infant Nutrition in Arlington, VA, United States. This page reflects FDA report H-0518-2026, dated March 4, 2026.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, plastic fragments can pose a choking risk or irritate and injure the digestive tract.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Plastic contamination

Possible health effects

Plastic fragments can pose a choking risk or cause irritation or injury to the mouth and digestive tract.

Higher-risk groups

Young children and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product and do not taste or chew it to check for fragments.
  2. 2Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Gerber Arrowroot Biscuits, NET WT recall?

Gerber Products Company Dba Nestle Infant Nutrition recalled Gerber Arrowroot Biscuits, NET WT in an FDA Class II enforcement action reported as H-0518-2026. Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag…

What injuries or health effects are linked to plastic contamination?

Plastic fragments can pose a choking risk or cause irritation or injury to the mouth and digestive tract.

Who is most at risk from Plastic contamination?

Young children and anyone who may swallow a fragment without noticing are at greater risk.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop eating or using the product and do not taste or chew it to check for fragments. Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Gerber Products Company Dba Nestle Infant Nutrition?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0518-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the Gerber Products Company Dba Nestle Infant Nutrition recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0518-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.