openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
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openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
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INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.
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.
These labels are deterministic app interpretations, not FDA categories.
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.
Code information
The affected lots of Integra¿ Spinal Trays were manufactured on 2/11/205 and on 7/11/2015. Lots: W1503004; S1501531; S1505556;
Distribution pattern
US Distribution to the states of : OH and CA. No foreign, Govt/VA/military consignee.