Howmedica Osteonics Corp.: Medical Device Recall in 2018 - (Recall #: Z-0810-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

AccuLIF TL Insertion Handle The AccuLIF Insertion Handle attaches to the implant and is specifically designed to allow a surgeon to insert the implant into the disc space with a fixed engagement between the two components to permit a controlled positioning of the implant in the anterior portion of the intervertebral space, and then through activation of the rotational pivot between the Handle and implant for final placement of the crescent-shaped cage across the anterior portion of the disc space. The AccuLIF TL Cages are indicated for intervertebral body fusion with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an adjunct to fusion in patients with degenerative disc disease (DOD) at one level or two contiguous levels from L2 to S1.

Product Classification:

Class II

Date Initiated: September 8, 2017

Date Posted: March 7, 2018

Recall Number: Z-0810-2018

Event ID: 79147

Reason for Recall:

When the lever of the Insertion Handle is in the "locked" position, the implant may be able to pivot rather than maintaining a rigid connection.

Status: Terminated

Product Quantity: 130

Code Information:

Model# 800804 Lot numbers 160010 and 170003

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated