Lower riskMedical device recall · FDA · Published April 9, 2020
Wright Medical INBONE Tibial Tray Recall: Missing Plasma Coating
Wright Medical recalls a specific lot of INBONE Tibial Trays due to missing plasma coating. This may affect patient mobility and joint function. Contact for details.
“Wright Medical INBONE Tibial Tray Recall: Missing Plasma Coating.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65458-wright-medical-inbone-tibial-tray-recall-missing-plasma-coating. Based on FDA recall #Z-1924-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1924-2020%22&limit=1).
The FDA announced on April 9, 2020, that Wright Medical Technology Inc. is recalling one lot of WRIGHT INBONE Tibial Trays because they are missing the plasma coating. The agency classified this as a Class II recall.
How to tell if you have it
Brand: Wright Medical
Product: WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left
REF: 2000252902
Lot code: 1619947
The hazard
One lot of INBONE Tibial Trays is missing the plasma coating. The product is intended to give a patient limited mobility by reducing pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.
Context
GovInfoNow's records show Wright Medical Technology, Inc. has 20 other recalls on record since March 14, 2018. Other recent recalls of similar products include Charlotte Claw Screw Recall (August 18, 2026), Stryker Infinity Resection Adjustment Block Recall (March 6, 2024), and Stryker Infinity Alignment Frame Distal Sub-Assembly Recall (June 13, 2023).
How to tell if you have this one
Check for the lot code 1619947 on the product. The recalled item is a specific size (2), left side, plasma spray type, with reference number 2000252902.
Brand
Wright Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the lot code 1619947 on the INBONE Tibial Tray to confirm if it is recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1924-2020 (April 9, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1924-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.