FDA Device recall Z-2684-2016
INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile by Integra Lifesciences D B A Integra Pain Management, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2684-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-04 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Integra Lifesciences D B A Integra Pain Management |
| Distribution | CA, OH, VA |
Product
INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.
Reason
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.
Identifiers
| code_info | The affected lots of Integra¿ Spinal Trays were manufactured on 2/11/205 and on 7/11/2015. Lots: W1503004; S1501531; S1505556; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2684-2016%22
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