RECALL RECORD — CLASS IIRecall closedF-0856-2013/FDA enforcement

Cocoa~latte Hot Drink Maker

What you need to know

Class II
  • What happened

    The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal bushing in the liquid containing vessel that may leach lead.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Lead is a toxic heavy metal with no safe blood lead level in children.

  • 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.

Recall closed · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameFocus Products Group LLC
Recalling firmFocus Products Group LLCLincolnshire, IL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • West Bend brand - model number 65032
  • Back to Basics brand - model numbers CM300BK, CM300BKL, CM300BLSS, CM300BR, CM300BR-BRL, CM300BRL and CM300W
Distribution area
Nationwide

Nationwide

United States

Quantity affected568, 000 units
Recall initiationFDA report date: January 9, 2013
FDA recall numberF-0856-2013

Beyond the headline

The recall, in context

Focus Products Group LLC initiated this food recall on November 17, 2012. The FDA enforcement report states: The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal bushing in the liquid containing vessel that may leach lead. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal bushing in the liquid containing vessel that may leach lead.

Cocoa~latte Hot Drink Maker was made or distributed by Focus Products Group LLC in Lincolnshire, IL, United States. This page reflects FDA report F-0856-2013, dated January 9, 2013.

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, lead is a toxic heavy metal with no safe blood lead level in children.

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

Lead contamination

Possible health effects

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

When symptoms may appear

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Higher-risk groups

Infants, young children, pregnant people and anyone with repeated exposure are at greatest risk.

What to do now

  1. 1Stop using or eating the affected product and prevent children from handling it.
  2. 2Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal.
  3. 3If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Do not use home remedies or ignore possible exposure; clinical testing is the appropriate next step.

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 Cocoa~latte Hot Drink Maker recall?

Focus Products Group LLC recalled Cocoa~latte Hot Drink Maker in an FDA Class II enforcement action reported as F-0856-2013. The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal bushing in the liquid containing vessel that may leach lead.

What injuries or health effects are linked to lead contamination?

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

How quickly can Lead contamination symptoms appear?

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Who is most at risk from Lead contamination?

Infants, young children, pregnant people and anyone with repeated exposure are at greatest 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 using or eating the affected product and prevent children from handling it. Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal. If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

How do I get a refund from Focus Products Group LLC?

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-0856-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Focus Products Group LLC 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-0856-2013. 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.