Alphatec Spine, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1821-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Atec Insignia Anterior Cervical Plate System, REF 136-0360 Insignia, ACP, 3-Level, 60 mm, Rx Only, Non-Sterile, UDI: (01)00190376268613

Product Classification:

Class II

Date Initiated: April 26, 2021

Date Posted: June 16, 2021

Recall Number: Z-1821-2021

Event ID: 87887

Reason for Recall:

There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.

Status: Terminated

Product Quantity: 1 units

Code Information:

8609327R

Distribution Pattern:

US Nationwide distribution in the states of FL, CA, IL, OK, TX, CT, IN, NC, WA, HI, ID, MA, SC, NM, and NY.

Voluntary or Mandated:

Voluntary: Firm initiated