FDA Device recall Z-1159-2019
Tibial Total Ankle Prosthesis Tray, Size 1, Product No. LJU221T
- FDA Device
- Class II
- terminated
- Published 2019-04-24
On 2019-04-24 the FDA classified a Class II recall of Tibial Total Ankle Prosthesis Tray, Size 1, Product No. LJU221T by Integra Lifesciences, citing the Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) an….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1159-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-08 |
| Published | 2019-04-24 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Integra Lifesciences |
| Distribution | AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK, PA, TX, VA, WA, WI |
Product
Tibial Total Ankle Prosthesis Tray, Size 1, Product No. LJU221T
Reason
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
Identifiers
| code_info | 180750 180860 180861 180892 181432 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1159-2019%22
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