Intrinsic Therapeutics, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2798-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid¿ ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral herniation, and confirmed by history, physical examination and imaging studies which demonstrate neural compression using MRI to treat a large annular defect (between 4-6 mm tall and between 6-10 mm wide) following a primary discectomy procedure (excision of herniated intervertebral disc) at a single level between L4 and S1.

Product Classification:

Class II

Date Initiated: July 24, 2020

Date Posted: August 19, 2020

Recall Number: Z-2798-2020

Event ID: 86121

Reason for Recall:

The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.

Status: Terminated

Product Quantity: 110 units

Code Information:

Catalog #: BAR-A8-8MM Part #: 2730815-A8 Lot #: 06112001, 06152001

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated