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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2041-2017 - Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Z-2042-2017 - Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Z-2046-2017 - Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching 2 05/05/2017 Arthrex, Inc.
Z-2044-2017 - Anthrex PEEK SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Z-2045-2017 - Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm 2 05/05/2017 Arthrex, Inc.
Z-2043-2017 - Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
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