Recall Z-2355-2020— Acuity Surgical Devices, LLC

Name: FDA recall Z-2355-2020
Creator: U.S. Food and Drug Administration
Published: 2019-01-07

Class II · Ongoing

Class II FDA medical device recall by Acuity Surgical Devices, LLC, initiated 2019-01-07. It names one FDA 510(k) clearance: K133827. Product: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbody 32x24x12 7 A Link Z Ti Unitary Open Interbody 32x24x12 12 A Link Z Ti Unitary Open Interbody 32x24x16 7 A Link Z Ti Unitary Open Interbody 32x24x16 12 Product Usage: is a spinal device that is implanted in the intervertebral body space via an anterior approach to improve stability of the spine while supporting fusion.. Reason: Due to a manufacturing process issue, it allowed vertebral body bone screws to not seat properly within the spinal device/cage..

Recalling firm: Acuity Surgical Devices, LLC
Classification: Class II
Status: Ongoing
Initiated: 2019-01-07
Firm location: Irving, TX, United States

510(k) clearances named in this recall

1 on FDA's record

K133827 — A-LINK ZOsteo Vasive, LLC·cleared 2014-11-17

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbody 32x24x12 7 A Link Z Ti Unitary Open Interbody 32x24x12 12 A Link Z Ti Unitary Open Interbody 32x24x16 7 A Link Z Ti Unitary Open Interbody 32x24x16 12 Product Usage: is a spinal device that is implanted in the intervertebral body space via an anterior approach to improve stability of the spine while supporting fusion.

Reason for recall

Due to a manufacturing process issue, it allowed vertebral body bone screws to not seat properly within the spinal device/cage.

Data sourced from openFDA. This site is unofficial and independent of the FDA.