RECALL RECORD — CLASS IIRecall closedF-0882-2013/FDA enforcement

Candy Canes, Peppermint Flavor, 5 OZ Boxes, Packed 12 Individually Candy Canes/box, and Labeled…

What you need to know

Class II
  • What happened

    Candy product may contain metal and/or plastic pieces embedded in the candy.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Metal fragments can cause cuts, choking or internal injury if swallowed.

  • 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

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand nameDollar Tree Distribution, INC.
Recalling firmDollar Tree Distribution, INC.Chesapeake, VA, United States
UPC / barcodes
01 880001 12052 101 880001 12060 5
Lot / date codes
  • Batch number: YT-0112003 01880-001 120521 01880-001 120605
Distribution area
Nationwide

Nationwide and Canada

United States, Canada

Quantity affected3, 147, 956 boxes
Recall initiationFDA report date: January 23, 2013
FDA recall numberF-0882-2013

Beyond the headline

The recall, in context

Dollar Tree Distribution, INC. initiated this food recall on December 21, 2012. The FDA enforcement report states: Candy product may contain metal and/or plastic pieces embedded in the candy. The FDA report lists distribution as: Nationwide and Canada.

The FDA enforcement report describes the reason as: Candy product may contain metal and/or plastic pieces embedded in the candy.

Candy Canes, Peppermint Flavor, 5 OZ Boxes, Packed 12 Individually Candy Canes/box, and Labeled… was made or distributed by Dollar Tree Distribution, INC. in Chesapeake, VA, United States. This page reflects FDA report F-0882-2013, dated January 23, 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, metal fragments can cause cuts, choking or internal injury if swallowed.

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

Metal contamination

Possible health effects

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product; do not try to find the fragment by tasting or chewing.
  2. 2Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain.
  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 Candy Canes, Peppermint Flavor, 5 OZ Boxes, Packed 12 Individually Candy Canes/box, and Labeled… recall?

Dollar Tree Distribution, INC. recalled Candy Canes, Peppermint Flavor, 5 OZ Boxes, Packed 12 Individually Candy Canes/box, and Labeled… in an FDA Class II enforcement action reported as F-0882-2013. Candy product may contain metal and/or plastic pieces embedded in the candy.

What injuries or health effects are linked to metal contamination?

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Who is most at risk from Metal contamination?

Children, older adults 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; do not try to find the fragment by tasting or chewing. Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Dollar Tree Distribution, 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-0882-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Dollar Tree Distribution, 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-0882-2013. 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

Brand history

More recalls by Dollar Tree Distribution, INC.

View brand

Related alerts

Recent Metal recalls

All alerts

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