Lower riskMedical device recall · FDA · Published February 2, 2023
Wright Medical recalls ORTHOLOC 3DSi CLAW II plates due to incorrect product mix-up
Wright Medical recalls ORTHOLOC 3DSi CLAW II 4-hole plates (Size 25mm, REF 40241425) sold with incorrect lot numbers. This mix-up means some packages contain the wrong product model.
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.
Wright Medical is recalling specific ORTHOLOC 3DSi CLAW II 4-hole plates (Size 25mm, REF 40241425) because two lots were mixed up during packaging. This means some packages contain the wrong product model, which could lead to incorrect use in bone fixation procedures. Read more at govinfonow.com/recall/58965-wright-medical-recalls-ortholoc-3dsi-claw-ii-plates-due-to.
“Wright Medical recalls ORTHOLOC 3DSi CLAW II plates due to incorrect product mix-up.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58965-wright-medical-recalls-ortholoc-3dsi-claw-ii-plates-due-to. Based on FDA recall #Z-1170-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1170-2023%22&limit=1).
The FDA announced on Feb. 2, 2023, that Wright Medical Technology is recalling ORTHOLOC 3DSi CLAW II 4 HOLE Plates due to packaging mix-ups containing incorrect products. The agency issued recall number Z-1170-2023 for the Class II device.
How to tell if you have it
Brand: Wright Medical
Product: ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
UPC: 00840420110770
Lot Number: 1636042
Units affected: 4
The hazard
Stryker identified that two specific lots of CLAW II plates were comingled, resulting in incorrect products in packages. Packaging for REF 40241425 incorrectly contained REF 402S0425, and vice versa.
Context
GovInfoNow's records show Wright Medical Technology has had 20 other recalls since March 14, 2018. Recent brand recalls include a Charlotte Claw Screw recall on Aug. 18, 2026, and a Stryker Infinity Resection Adjustment Block recall on March 6, 2024. Other recent recalls of similar products include an Encore Medical EMPOWR 3D Knee Tibial Insert recall (Jan. 5, 2026) and packaging mix-up recalls for the same product line (Feb. 16, 2026).
How to tell if you have this one
Check for the product name ORTHOLOC 3DSi CLAW II 4-hole plate, Size 25mm, REF 40241425. Look for Lot Number 1636042 or similar incorrect packaging where 402S0425 was mixed with 40241425.
Brand
Wright Medical
Product
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
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 in the state of NY.
Recall number
Product, codes & lots
Quantity
Z-1169-2023
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device; GTIN 00840420152985, Lot Number 1636048
10 units
Z-1170-2023
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device; GTIN 00840420110770, Lot Number 1636042
4 units
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product's lot number and reference code to ensure it matches the correct model (40241425) and lot (1636042).
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 34 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-1170-2023 (February 2, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1170-2023 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.