Use cautionMedical device recall · FDA · Published June 29, 2022
DePuy ATTUNE Sizing Guide Recall: Corroded Spring Risks Surgical Complications
DePuy recalls ATTUNE Measured Sizing and Rotation Guides made with incorrect steel spring that may corrode, causing surgical delays, debris, and joint issues. Affected units include specific lot numbers and part numbers.
Manufactured with a Galvanized High Carbon Steel spring instead of the correct 302 Stainless steel spring. has the potential to oxidize and corrode in the ATTUNE Measured Sizing & Rotation Guide, resulting in surgical delay, debris in surgical field, Osteolysis, Poor Joint Mechanics, Soft Tissue Irritation, Pain
Take action
Contact the company
📍Recalling firmDePuy Orthopaedics, Inc.700 Orthopaedic Dr · Warsaw, IN 46582-3994
“DePuy ATTUNE Sizing Guide Recall: Corroded Spring Risks Surgical Complications.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/60406-depuy-attune-sizing-guide-recall-corroded-spring-risks-surgical-complications. Based on FDA recall #Z-1419-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1419-2022%22&limit=1).
The FDA announced on June 29, 2022, that DePuy Orthopaedics, Inc. is recalling the ATTUNE Measured Sizing and Rotation Guide due to a spring material defect. The company has initiated this voluntary Class II recall.
How to tell if you have it
Brand: DePuy
Product: ATTUNE Measured Sizing and Rotation Guide
Part Number: 254400525
UPC/GTIN: 10603295434061
Lot Codes: AB4536235, AB4733296, AB4841493, AB4810808, AB4841495, AB4904565, AB4967214, AB5004557, and AB5034303
The hazard
The device was manufactured with a Galvanized High Carbon Steel spring instead of the correct 302 Stainless steel spring. This defect has the potential to oxidize and corrode, resulting in surgical delay, debris in the surgical field, Osteolysis, Poor Joint Mechanics, Soft Tissue Irritation, or Pain.
Context
GovInfoNow's records show DePuy Orthopaedics, Inc. has 23 other recalls on record since July 12, 2017. Other recent recalls of similar products include Depuy ATTUNE Revision Hinge Knee Insert Components (May 19, 2026) and Howmedica TRIATHLON Hinge Insert Recall (July 30, 2026).
How to tell if you have this one
Check the product label for part number 254400525 or GTIN 10603295434061. Affected units include specific lot numbers: AB4536235, AB4733296, AB4841493, AB4810808, AB4841495, AB4904565, AB4967214, AB5004557, and AB5034303.
Brand
DePuy
Product
ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for part number 254400525 or GTIN 10603295434061 on the guide.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide Foreign: Argentina, Australia, Austria, Bahrain, Belgium, Brazil, Canada, Chile, China, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Lithuania,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 28 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-1419-2022 (June 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1419-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.