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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2037-2018 - LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a. Product Code LS-12; b. Product Code LS-13; c. Product Code LS-14; d. P... 2 05/31/2018 Torax Medical, Inc.
Z-2038-2018 - LINX Reflux Management System, Implant Clasp, 12-17 Bead, 0.7T, Product Code LXC-xx, sterile, Rx only. Labeled as: a. Product Code LXC-12; b. Product Code LXC-13; c. Product Code LXC-14; d... 2 05/31/2018 Torax Medical, Inc.
Z-2041-2018 - LINX Reflux Management System, Implant Clasp, 13-16 Bead, 1.5T, Product Code LXM-xx, sterile, Rx only. Labeled as: a. Product Code LXM-13; b. Product Code LXM-14; c. Product Code LXM-15; d... 2 05/31/2018 Torax Medical, Inc.
Z-2040-2018 - LINX Reflux Management System, Implant Clasp, 12-17 Bead, 0.7T, Product Code LX-xx, sterile, Rx only. Labeled as: a. Product Code LX-12; b. Product Code LX-13; c. Product Code LX-14; d. Pr... 2 05/31/2018 Torax Medical, Inc.
Z-2039-2018 - LINX Reflux Management System, Implant Clasp, 13-17 Bead, 1.5T, Product Code LXMC-xx, sterile, Rx only. Labeled as: a. Product Code LXMC-13; b. Product Code LXMC-14; c. Product Code LXMC-15; ... 2 05/31/2018 Torax Medical, Inc.
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