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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 500 Results *
Recall Date to: 08/30/2015
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BIOMET 3i LOCATOR ABUTMENT, Catalog/Item Number: LOA003, 3.0mm, BioMet 3i , Palm Beach, FL. 3 06/25/2015 Biomet 3i, Inc.
BIOMET 3i LOCATOR ABUTMENT, Catalog/Item Number: LOA002, 2.0mm, BioMet 3i, Palm Beach, FL. 3 06/25/2015 Biomet 3i, Inc.
Medtronic MiniMed Paradigm Model 712 3 06/25/2015 Medtronic MiniMed
Medtronic MiniMed Paradigm Model 512 3 06/25/2015 Medtronic MiniMed
Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK... 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.
Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length ... 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

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