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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 250 Results
510(K) Number: K100238
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Product Description
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FDA Recall
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Affixus Hip Fracture Nail Left 125 9 mm x 440 mm, Item Number 814409440 Product Usage: Intended ... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 125 9 mm x 460 mm, Item Number 814409460 Product Usage: Intended ... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 125 Deg 11x300mm, Item Number 814411300 The Affixus Hip Fracture ... 2 11/14/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 125 Deg 9x165mm, Item Number 816709165 The Affixus Hip Fracture N... 2 11/14/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 11 mm x 360 mm, Item Number 814611360 Product Usage: Intended... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 11 mm x 380 mm, Item Number 814611380 Product Usage: Intend... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 11 mm x 400 mm, Item Number 814611400 Product Usage: Intended... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 15 mm x 360 mm, Item Number 814615360 Product Usage: Intended... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 9 mm x 360 mm, Item Number 814609360 Product Usage: Intende... 2 10/18/2018 Zimmer Biomet, Inc.
Affixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture ... 2 11/14/2018 Zimmer Biomet, Inc.
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