Amendia, Inc recalls

11 recalls on record · latest: July 7, 2017

Official U.S. recall history for Amendia, Inc, compiled from official government records.

Get recall alerts

Free email alert whenever Amendia, Inc has a new recall — straight from official government data. Unsubscribe anytime.

Amendia, Inc recalls Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are intended to b…

July 7, 2017 · Medical device recalls Moderate risk Incorrect direct marking and color identification for the affected lot of Ceres…

Mac Pin Non-Cannulated Screw recalled over labeling errors

July 7, 2017 · Medical device recalls Moderate risk Incorrect labeling for the lot of MAC Pins. Although the pins are laser as 460…

Amendia product recalled over labeling errors

April 6, 2017 · Medical device recalls Moderate risk Mislabeled guide wires - It was discovered that some Guide Wires labeled as sta…

Amendia, Inc recalls K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U; K-Wire Threaded 1.4mm x 18, Part Number 9080-18T; K-Wire Non-Th…

November 22, 2016 · Medical device recalls Moderate risk The rods are packaged in packages with unacceptable seals. In some cases, the i…

Amendia, Inc recalls Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part Number TBS025; Black Widow 6.6…

November 22, 2016 · Medical device recalls Moderate risk There is a problem with the mating feature between the plate and screw which co…

Amendia, Inc recalls Zeus-P Lumbar Interbody Device

November 22, 2016 · Medical device recalls Moderate risk Labeling error where three boxes in inventory had conflicting patient and prima…

Amendia, Inc recalls Dual Stylet Needle, Part Number 812-11R-15 The guide wire is passed through the cannulated handle of the Dual Stylet Ne…

November 22, 2016 · Medical device recalls Moderate risk The rods are packaged in packages with unacceptable seals. In some cases, the i…

Amendia, Inc recalls Optimus Fixed Awl

November 22, 2016 · Medical device recalls Moderate risk Complaints that the tip of the awl broke after impaction during surgery.

Amendia, Inc recalls Savannah-T Straight Rod, 200mm, Part Number 10704-200; Savannah-T Straight Rod, 250mm, Part Number 10704-250; Savannah…

November 22, 2016 · Medical device recalls Moderate risk The rods are packaged in packages with unacceptable seals. In some cases, the i…

Amendia, Inc recalls Black Widow Plate 19mm Plate, Part Number TBP119; Black Widow Plate 23mm Plate, Part Number TBP123 The Black Widow Butt…

November 22, 2016 · Medical device recalls Moderate risk There is a problem with the mating feature between the plate and screw which co…