INTEGRA Spinal Tray — Class II medical device recall Z-2684-2016
Terminated recall by Integra LifeSciences Corp. d.b.a. Integra Pain Management, reported 2016-09-07, distributed in CA, OH. Integra LifeSciences is recalling Spinal Trays, Cat No. 3404875, because of the affected recalled Hospira 5% L
| Recall number | Z-2684-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp. d.b.a. Integra Pain Management, Salt Lake City, UT, United States |
| Recall initiated | 2016-08-04 |
| Classified | 2016-08-29 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2016-12-19 |
| Distributed | CA, OH |
| Lot numbers | S1501531, S1505556, W1503004 |
| Model numbers | 3404875 |
Product
INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.
Reason for recall
Integra LifeSciences is recalling Spinal Trays, Cat No. 3404875, because of the affected recalled Hospira 5% Lidocaine HCL that is a component of some lots of the Spinal Trays.
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-2684-2016. 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.