Lower riskMedical device recall · FDA · Published April 10, 2023
Wright Medical ORTHOLOC 3Di Fusion Plate Recall: Incorrect Laser Marking
Wright Medical recalls specific OrthoLoc 3Di Fusion plates with incorrect dorsiflexion laser markings. Affected units may have improper alignment risks during bone surgery.
“Wright Medical ORTHOLOC 3Di Fusion Plate Recall: Incorrect Laser Marking.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/58591-wright-medical-ortholoc-3di-fusion-plate-recall-incorrect-laser-marking. Based on FDA recall #Z-1467-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1467-2023%22&limit=1).
Wright Medical Technology, Inc. voluntarily recalled stryker ORTHOLOC 3Di Fusion Plate MTP Right bone stabilization devices due to incorrect dorsiflexion descriptions laser marked on two lots, the FDA said on April 10, 2023.
How to tell if you have it
stryker ORTHOLOC 3Di Fusion Plate MTP Right
REF 58A221RT
UDI/DI 00889797101035
Lot Number 1737413
The hazard
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts, according to the FDA.
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 EMPOWR 3D KNEE Implants Have Incorrect Labeling (Jan. 15, 2026), Orthof: Minirail Fixator M122 Labeled Incorrectly (June 10, 2026), and Encore Medical RSP Humeral Socket Insert Recall: Incorrect Labeling Hazard (Jan. 15, 2026).
How to tell if you have this one
Check for the model 'ORTHOLOC 3Di Fusion Plate MTP Right' with reference number REF 58A221RT. The specific lot number 1737413 is affected, and the units were sold with UDI/DI 00889797101035.
Brand
Wright Medical
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
Z-1466-2023
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation; UDI/DI 00889797101011, Lot Number 1736809
41 units
Z-1467-2023
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation; UDI/DI 00889797101035, Lot Number 1737413
50 units
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product model, reference number, and lot number to confirm if it matches the recalled items.
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 published this recall 23 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
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-1467-2023 (April 10, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1467-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.