Brand
Amendia, Inc Recalls
9 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Amendia, Inc.
9Total Recalls
0Critical
7,343Units Affected
Jul 7, 2017Most Recent
All Recalls
Every Amendia, Inc Recall
Sorted by most recent. Click any recall for full details.
9 recalls
High RiskFDA
Amendia, Inc
Mac Pin Non-Cannulated Screw, 6.5 x 60mm
Medical Devices41 affectedJul 7, 2017
High RiskFDA
Amendia, Inc
01.4mm x 457mm (18in) K-Wire, Threaded Blunt, Ref 9080B-18T, Qty: 1 per pack, Material: SS 316L, Full Temper, per ASTM F138, Amendia, 17...
Medical Implants15 affectedApr 6, 2017
High RiskFDA
Amendia, Inc
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-Threaded 1.4mm x 18,...
Medical Devices5,833 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part Number TBS025; Black Widow 6.6mm x 30mm Screw, P...
Medical Devices96 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Zeus-P Lumbar Interbody Device
Medical Devices25 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Dual Stylet Needle, Part Number 812-11R-15 The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed...
Medical Devices1,078 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Optimus Fixed Awl
Medical Devices9 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Savannah-T Straight Rod, 200mm, Part Number 10704-200; Savannah-T Straight Rod, 250mm, Part Number 10704-250; Savannah T-Straight Rod 300...
Medical Devices240 affectedNov 22, 2016
High RiskFDA
Amendia, Inc
Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skel...
Medical Devices6 affectedNov 22, 2016