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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K831005
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Product Description
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FDA Recall
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G-PIN 2.8BL 3.2PL 98CM 2PK; 467260 NL DRIVING GUIDE 4.4MM X 80CM; 467220 Intended to be used as... 2 06/01/2018 FEI # 1825034
Zimmer Biomet, Inc.
BEAD TIP GD WIRE 3.0MM X 60CM; 29402 Intended to be used as a guide pin for insertion of implan... 2 06/01/2018 FEI # 1825034
Zimmer Biomet, Inc.
3.2MM X 510MM COCR THD TIP; 14-443053 Intended to be used as a guide pin for insertion of implan... 2 06/01/2018 FEI # 1825034
Zimmer Biomet, Inc.
RECON DRILL 6MM X 439MM; 14-443023 Intended to be used as a guide pin for insertion of implants ... 2 06/01/2018 FEI # 1825034
Zimmer Biomet, Inc.
Uniflex Humeral Nail: 467265 G-PIN 2.8BL 3.2PL 60CM 2PK Pin, Fixation, Smooth A 467265-01 Ball T... 2 10/14/2016 FEI # 1825034
Zimmer Biomet, Inc.
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