Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 07/24/2014 510(K) Number: K052585 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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