PlainRecalls
FDA Devices Moderate Class II Terminated

Cypher MIS Screw System-The system includes screws, various types and sizes of rods, and set screws. Various instruments are also available for use by the surgeon to facilitate implantation of the device. Non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion.

Reported: January 14, 2015 Initiated: October 8, 2014 #Z-0909-2015

Product Description

Cypher MIS Screw System-The system includes screws, various types and sizes of rods, and set screws. Various instruments are also available for use by the surgeon to facilitate implantation of the device. Non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion.

Reason for Recall

Inoperative screw head seat splay and/or fracture as a result of positioning of the rod which is a part of the Cypher MIS Screw System.

Details

Recalling Firm
Ebi, Llc
Units Affected
2816 approx.units ( 2688 units US and 128 OUS)
Distribution
Worldwide Distribution: US Distribution to states of: AL, CA, CT, IN, LA, NC, NJ TX & WI; and the country of: The Netherlands.
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Cypher MIS Screw System-The system includes screws, various types and sizes of rods, and set screws. Various instruments are also available for use by the surgeon to facilitate implantation of the device. Non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion.. Recalled by Ebi, Llc. Units affected: 2816 approx.units ( 2688 units US and 128 OUS).
Why was this product recalled?
Inoperative screw head seat splay and/or fracture as a result of positioning of the rod which is a part of the Cypher MIS Screw System.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 14, 2015. Severity: Moderate. Recall number: Z-0909-2015.