RECALL RECORD — CLASS IIRecall closedF-0899-2019/FDA enforcement
1908 Brands·Food·Jan 30, 2019

Bundle Organics Bar Oatmeal Raisin, 1.9 OZ Snack Bar, Ambient Storage

What you need to know

Class II
  • What happened

    Bundle Organics snack bars are recalled due to the presence of mold.

  • Health risk

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

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Product identification

Source: FDA FOOD

Brand name1908 Brands
Recalling firm1908 BrandsLongmont, CO, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot # s 2913, 2890
Distribution area
VA

Distributed to One consignee. No foreign/VA/govt/military consignees.

United States

Quantity affected3045 bars
Recall initiationFDA report date: February 20, 2019
FDA recall numberF-0899-2019

Beyond the headline

The recall, in context

1908 Brands initiated this food recall on January 30, 2019. The FDA enforcement report states: Bundle Organics snack bars are recalled due to the presence of mold. The FDA report lists distribution as: Distributed to One consignee. No foreign/VA/govt/military consignees.

The FDA enforcement report describes the reason as: Bundle Organics snack bars are recalled due to the presence of mold.

Bundle Organics Bar Oatmeal Raisin, 1.9 OZ Snack Bar, Ambient Storage was made or distributed by 1908 Brands in Longmont, CO, United States. This page reflects FDA report F-0899-2019, dated February 20, 2019.

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, visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

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 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 Bundle Organics Bar Oatmeal Raisin, 1.9 OZ Snack Bar, Ambient Storage recall?

1908 Brands recalled Bundle Organics Bar Oatmeal Raisin, 1.9 OZ Snack Bar, Ambient Storage in an FDA Class II enforcement action reported as F-0899-2019. Bundle Organics snack bars are recalled due to the presence of mold.

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 1908 Brands?

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-0899-2019 and keep the packaging, lot code and proof of purchase if you have them.

Is the 1908 Brands 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-0899-2019. 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.