Beekley Corporation recalls O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography.
- Recall date
- June 13, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2830-2018
- FDA classification
- Class II
- Brand / firm
- Beekley Corporation
- Sold / distributed
- Worldwide Distribution: US (Nationwide) and countries of; AUSTRALIA, AUSTRIA, BAHRAIN, CANADA, GREAT BRITAIN, ISRAEL, SAUDI ARABIA, SOUTH AFRICA & UNITED ARAB EMIRATES.
Why it was recalled
There is a potential for imaging artifact to mimic calcifications on patient's mammograms
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography.
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