Bella Blanket Protective Coverlet — Class II medical device recall Z-2080-2012
Terminated recall by Beekley Corporation, reported 2012-08-01, distributed nationwide. Imaging artifact can occur on mammogram result
| Recall number | Z-2080-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beekley Corporation, Bristol, CT, United States |
| Recall initiated | 2012-07-02 |
| Classified | 2012-07-26 |
| Reported by FDA | 2012-08-01 |
| Terminated | 2013-07-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, JP |
| Quantity | 86,000 units |
| Lot numbers | 107657, 108150, 108833 |
Product
Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plate.
Reason for recall
Imaging artifact can occur on mammogram result
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2080-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.