Beekley Altus Floral Skin Markers Recalled for Separation Defect
Beekley Corporation is recalling 6,420 units of Altus Floral Skin Markers because the marker may separate from the backing material.
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 defect involves a physical separation of the marker from its backing. No injuries or illnesses are reported in the source text, fitting the criteria for a moderate severity recall involving a potential functional defect.
Plain-English summary
Beekley Corporation is recalling 6,420 units of Beekley Altus Floral Skin Markers, Lot A004. These disposable skin markers are designed for digital mammography to mark areas of concern or pain. The recall was initiated because the digital skin mammography marker may separate from the backing of the spot material.
The affected products were distributed nationwide in the United States. Beekley Corporation is the recalling firm.
Consumers who have these specific skin markers should stop using them and contact the manufacturer for instructions on return or replacement.
The recalled product
- Product
- Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain
- Manufacturer
- Beekley Corporation
- Hazard
- Affected units
- 6,420
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 (1)
- Lot Numbers: A004
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by Beekley Corporation under a single FDA (Devices) 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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