Beekley S-Spots Floral Skin Markers Recalled for Separation Defect
Beekley Corporation is recalling 36,518 units of S-Spots Floral Skin Markers because the digital skin 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 source text does not report any hospitalizations, injuries, or illnesses, fitting the criteria for a moderate severity recall involving a functional defect without reported harm.
Plain-English summary
Beekley Corporation is recalling 36,518 units of S-Spots Floral Skin Markers, which are used for marking moles, scars, palpable masses, or areas of concern during mammography. 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. The recall includes units with lot numbers A020, A021, A022, A023, A024, AO25, and A026. The source text does not specify a date range for distribution or report any specific injuries or illnesses associated with this defect.
Consumers and healthcare providers should stop using the affected markers and contact Beekley Corporation for further instructions or a refund. The source text does not provide specific contact details for the recall firm.
The recalled product
- Product
- Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern
- Manufacturer
- Beekley Corporation
- Hazard
- Affected units
- 36,518
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 (7)
- Lot Numbers: A020
- A021
- A022
- A023
- A024
- AO25
- A026
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.
See all 4 products in this recall →Related recalls
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