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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 01/30/2015 510(K) Number: K052585
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Product Description
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FDA Recall
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LATERAL BIOPSY PLATE - For use with the Liberty 9000, 8-Channel Breast Coil. The Lateral Biopsy pla... 2 02/15/2007 USA Instruments Incorporated
The recalled product is the medial biopsy plate, part #2414342. The biopsy plate is labeled in part:... 2 02/15/2007 USA Instruments Incorporated
The recalled product is the Large grid biopsy plate, part #2414797. The biopsy plate is labeled in p... 2 02/15/2007 USA Instruments Incorporated
The recalled product is the Disposable biopsy plate, part #U1-150131. The biopsy plate is labeled in... 2 02/15/2007 USA Instruments Incorporated
The recalled product is the Lateral biopsy plate, part #2414346. The biopsy plate is labeled in part... 2 02/15/2007 USA Instruments Incorporated
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