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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 500 Results *
Recall Date to: 07/05/2015
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Product Description
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Medtronic MiniMed Paradigm Model 512 3 06/25/2015 Medtronic MiniMed
Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length ... 3 06/11/2015 Biomet, Inc.
Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma... 3 06/11/2015 Biomet, Inc.
MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM ... 3 06/11/2015 Biomet, Inc.
Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK... 3 06/11/2015 Biomet, Inc.
RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter -... 3 06/09/2015 Acclarent, Inc.
VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. ... 3 06/04/2015 ORTHO-CLINICAL DIAGNOSTICS
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

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