Barricaid Annual Closure Device — Class II medical device recall Z-2798-2020
Terminated recall by Intrinsic Therapeutics, Inc., reported 2020-08-19, distributed nationwide. The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box)
| Recall number | Z-2798-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intrinsic Therapeutics, Inc., Woburn, MA, United States |
| Recall initiated | 2020-07-24 |
| Classified | 2020-08-13 |
| Reported by FDA | 2020-08-19 |
| Terminated | 2020-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 110 units |
| Reason classes | labeling |
| Lot numbers | 06112001, 06152001 |
| Model numbers | 2730815-A8, BAR-A8-8MM |
Product
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.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2798-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.