RECALL RECORD — CLASS IIIRecall closedF-1324-2013/FDA enforcement

Gerber¿ Pure Water (1 Plastic Gallon)

What you need to know

Class III
  • What happened

    An audit to the purified water supplier revealed deficiencies related to the Ozone purification system and particulates, the analytical results show that mold was found on one…

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameNestle Puerto Rico INC
Recalling firmNestle Puerto Rico INCCatano, PR, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Manufactured- 2/20/13 - 3/22/13- 3.79L (1 Gallon) 1304948683, 1305048682, 1305048683, 1305148682, 1305348683, 1305648682, 1305648683, 1305748682, 1306048682, 1306348681, 1306548682, 1306648681, 1306748682, 1307048682, 1307348681
Distribution area
IN

Product was distributed in Puerto Rico only (wholesalers and distributors).

United States, Puerto Rico

Quantity affected12, 948 - (3 gallons cases)
Recall initiationFDA report date: April 24, 2013
FDA recall numberF-1324-2013

Beyond the headline

The recall, in context

Nestle Puerto Rico INC initiated this food recall on March 19, 2013. The FDA enforcement report states: An audit to the purified water supplier revealed deficiencies related to the Ozone purification system and particulates, the analytical results show that mold was found on one of the batches. The FDA report lists distribution as: Product was distributed in Puerto Rico only (wholesalers and distributors).

The FDA enforcement report describes the reason as: An audit to the purified water supplier revealed deficiencies related to the Ozone purification system and particulates, the analytical results show that mold was found on one of the batches

Gerber¿ Pure Water (1 Plastic Gallon) was made or distributed by Nestle Puerto Rico INC in Catano, PR, United States. This page reflects FDA report F-1324-2013, dated April 24, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 lot and date codes 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

Mold contamination

Symptoms to watch for

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Higher-risk groups

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Visible mold can indicate a moisture, packaging or temperature failure.

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¿ Pure Water (1 Plastic Gallon) recall?

Nestle Puerto Rico INC recalled Gerber¿ Pure Water (1 Plastic Gallon) in an FDA Class III enforcement action reported as F-1324-2013. An audit to the purified water supplier revealed deficiencies related to the Ozone purification system and particulates, the analytical results show that mold was found on one…

What are the symptoms of Mold contamination exposure?

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Who is most at risk from Mold contamination?

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Nestle Puerto Rico INC?

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 F-1324-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Nestle Puerto Rico INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1324-2013. 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

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