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U.S. Department of Health and Human Services

Medical Device Recalls

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71 to 80 of 500 Results *
Recall Date to: 07/14/2014
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Product Description
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FDA Recall
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6 DEGREE COCR FEM HEAD 36 2 02/20/2014 Zimmer, Inc.
MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID 2 02/20/2014 Zimmer, Inc.
CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes) 2 02/20/2014 Zimmer, Inc.
FEM HD ION (various sizes) 2 02/20/2014 Zimmer, Inc.
HERBERT BONE SCREW, 3.0MM and HERBERT CANNULATED BONE S 2 02/20/2014 Zimmer, Inc.
COMPRESSION SCREW (1/2, 1-1/2, 1-1/4, 1-3/4, 1. 2. 3/4 IN) 2 02/20/2014 Zimmer, Inc.
Magna-Fx Cannulated Screw Fixation System 7.0 mm. Item codes starting with 0011420, 11460 and 11461. 2 02/20/2014 Zimmer, Inc.
HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Items starting with 0011500 and 0011520. 2 02/20/2014 Zimmer, Inc.
FREE-LOCK LAG SCREW, 12.7, FREE-LOCK LAG SCREW, 15.8, FREE-LOCK SUPRACOND TUBE and FREE-LOCK TUBE & ... 2 02/20/2014 Zimmer, Inc.
Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM, LAG SCR 12.7D X 55 MM SHO... 2 02/20/2014 Zimmer, Inc.

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