BEUDAMED
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    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; d. Product Code LXMC-16; e. Product Code LXMC-17; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed with Gastroesophageal Reflux Disease (GERD) as defined by abnormal pH testing, and who are seeking an alternative to continuous acid suppression therapy (i.e. proton pump inhibitors or equivalent) in the management of their GERD.

    FDA Recall
    Terminated ·Torax Medical, Inc.·Product code LEI·April 20, 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. Product Code LXM-16; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed with Gastroesophageal Reflux Disease (GERD) as defined by abnormal pH testing, and who are seeking an alternative to continuous acid suppression therapy (i.e. proton pump inhibitors or equivalent) in the management of their GERD.

    FDA Recall
    Terminated ·Torax Medical, Inc.·Product code LEI·April 20, 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. Product Code LX-15; e. Product Code LX-16; f. Product Code LX-17; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed with Gastroesophageal Reflux Disease (GERD) as defined by abnormal pH testing, and who are seeking an alternative to continuous acid suppression therapy (i.e. proton pump inhibitors or equivalent) in the management of their GERD.

    FDA Recall
    Terminated ·Torax Medical, Inc.·Product code LEI·April 20, 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. Product Code LS-15; e. Product Code LS-16; f. Product Code LS-17; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed with Gastroesophageal Reflux Disease (GERD) as defined by abnormal pH testing, and who are seeking an alternative to continuous acid suppression therapy (i.e. proton pump inhibitors or equivalent) in the management of their GERD.

    FDA Recall
    Terminated ·Torax Medical, Inc.·Product code LEI·April 20, 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. Product Code LXC-15; e. Product Code LXC-16; f. Product Code LXC-17; Laparoscopic, fundic-sparing anti-reflux procedure indicated for patients diagnosed with Gastroesophageal Reflux Disease (GERD) as defined by abnormal pH testing, and who are seeking an alternative to continuous acid suppression therapy (i.e. proton pump inhibitors or equivalent) in the management of their GERD.

    FDA Recall
    Terminated ·Torax Medical, Inc.·Product code LEI·April 20, 2018

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584003;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001380;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001635;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000759;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001878;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000479;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001417;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000781;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000305;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001423;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000477;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000628;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001579;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002075;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001157;

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024