Mel-O Cream Donuts Recalls Arrowhead Shells Due to Fingertip Contamination
Mel-O Cream Donuts International is recalling 20 cases of Arrowhead/Christmas Tree Shells because a human fingertip was found in the product filling line.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a foreign object (human fingertip) without reported illnesses or injuries, fitting the criteria for moderate severity.
Plain-English summary
Mel-O Cream Donuts International, Inc. is voluntarily recalling 20 cases of Arrowhead/Christmas Tree Shells. The product is identified by the Best If Used By date of 02/26/2017, Batch 162734737, and Product Code 23520. Each case contains approximately 96 units and weighs 12 pounds.
The recall was initiated after a human fingertip was found in the product filling line. This is a Class II recall, indicating a situation that might cause temporary or medically reversible health adverse effects.
The affected product was distributed in Wisconsin, Illinois, and Ohio. Consumers who have this product should check their pantries for the specific batch and date codes listed above. If found, consumers should discard the product or return it to the place of purchase.
The recalled product
- Product
- Arrowhead/Christmas Tree Shells; Best If Used By 02/26/2017; Batch 162734737; NET WT 12 Pounds; Approximate Unit Count [Per Case]: 8 Dozen [96 units]
- Manufacturer
- Mel-O Cream Donuts International, Inc.
- Category
- Food — Baked Goods
- Hazard
- Affected units
- 20
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Product Code: 23520
- Batch: 162734737
- UPC: 4792423520
- Best If Used By 02/26/2017
Distribution
Part of a larger recall action
This product is one of 9 recalled by Mel-O Cream Donuts International, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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