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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 500 Results *
Recall Date to: 09/03/2015
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Product Description
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FDA Recall
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Volk 25D Large Clear BIO Lens with case UPC: 8 11608 01010 6, VOLK OPTICAL INC. The Volk Optical BI... 3 05/28/2015 Volk Optical Inc
D2-40 (Lymphatic Marker); For In Vitro Diagnostic; Catalog number: PM266AA Product Usage: In Vi... 3 05/26/2015 Biocare Medical, LLC
Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer Surgical, Inc. Inte... 3 05/13/2015 Zimmer Surgical Inc
Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprise... 3 05/11/2015 Spinal Elements, Inc
ThermoFlo 1 HME, Disposable, Non-sterile, Expiry date 04/17. Used as a humidifier in a breathing... 3 05/09/2015 Arc Medical Inc
Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be us... 3 05/07/2015 Stryker Instruments Div. of Stryker Corporation
Vitek 2 AST-P635 REF 416 911 Gram Positive Susceptibility Card, 20 cards per container, IVD. Int... 3 04/08/2015 Biomerieux Inc
Vitek 2 AST-P640 REF 418 579 Gram Positive Susceptibility Card, 20 cards per container, IVD. Int... 3 04/08/2015 Biomerieux Inc
Vitek 2 AST-P641 REF 418 590 Gram Positive Susceptibility Card, 20 cards per carton, IVD. Intend... 3 04/08/2015 Biomerieux Inc
cobas® EGFR Mutation Test epidermal growth factor receptor (EGFR) gene DNA assay 3 03/25/2015 Roche Molecular Systems, Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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