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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K953385
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Product is labeled in part: "***REF: 01-7036, LOT 999999, "1.5MM" SYSTEM PLATE L-SHAPE, 3 X 3 HOL... 2 03/23/2012 FEI # 1032347
Biomet Microfixation, LLC
"***REF: 91-6704***THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM (.059X.159") (WXL)***TI... 2 07/22/2011 FEI # 1032347
Biomet Microfixation, Inc.
***BIOMET MICROFIXATION BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.bio... 2 05/27/2011 FEI # 1032347
Biomet Microfixation, Inc.
BIOMET MICROFIXATION "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, QTY 1, 1.5 X 4MM TITANIUM. ... 3 08/11/2010 FEI # 1032347
Biomet Microfixation, Inc.
BIOMET MICROFIXATION REF: 91-6103 "1.5MM" SYSTEM HIGH TORQUE (HT), SD, X-DR, SCREW 1.5MM X 3.5MM (W... 3 06/30/2010 FEI # 1032347
Biomet Microfixation, Inc.
BIOMET MICROFIXATION, "1.5MM" SYSTEM BONE SCREW LP, SELF DRILL, X-DRIVE, SGL.LEAD AUGER POINT, 1.5 ... 3 03/17/2010 FEI # 1032347
Biomet Microfixation, Inc.
Package of center-drive bone screws labeled in part: "***REF: 01-7204***1.5MM" SYSTEM CENTER-DRIVE ... 3 01/23/2012 FEI # 1032347
Biomet Microfixation, Inc.
Package of cross-drive bone screws labeled in part: "***REF #95-1504***"1.5MM" SYSTEM HIGH TORQUE (H... 3 01/23/2012 FEI # 1032347
Biomet Microfixation, Inc.
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