Lower riskMedical device recall · FDA · Published June 2, 2022
Stryker INFINITY Resect Guide Color Coding Recall: Incorrect Color Coding
Stryker recalls INFINITY Resect Guide for INBONE Talus, Size 4 (Model #33620254) due to incorrect color coding. This may cause confusion during surgical procedures. Affected units were sold with Lot #2039558 and GTIN 00889797006552.
“Stryker INFINITY Resect Guide Color Coding Recall: Incorrect Color Coding.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60557-stryker-infinity-resect-guide-color-coding-recall-incorrect-color-coding. Based on FDA recall #Z-1291-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1291-2022%22&limit=1).
Wright Medical Technology, Inc. recalled the Stryker INFINITY Resect Guide for INBONE Talus, Size 4 due to incorrect color coding, according to the FDA on June 2, 2022.
How to tell if you have it
Stryker INFINITY Resect Guide for INBONE Talus, Size 4
Model #33620254
Lot #2039558
UPC 00889797006552
The hazard
The instrument is incorrectly color coded, according to the FDA.
Context
GovInfoNow's records show Wright Medical Technology, Inc. has had 20 other recalls on record since March 14, 2018. Other recent recalls of similar products include Stryker MOLLI 2 System Recall (Jan. 21, 2026), Stryker CHROMOPHARE Softlit Ring Surgical Light Recall (Feb. 23, 2026), and XTANT Medical Xpress Pedicle Screw System (Feb. 18, 2026).
How to tell if you have this one
Check for the model number 33620254 on the instrument. The product was sold with Lot #2039558 and GTIN 00889797006552. This instrument is non-sterile and used with the INFINITY Total Ankle System.
Brand
Stryker
Product
Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Instrument Model
Look for the model number 33620254 on the instrument to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 18 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, MA, MI, MN, MO, NC, NY, OH, PA, TX, and WA. The countries of Australia, Belgium, Canada, France, Germany, Hong Kong, Israel, Sweden,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Iowa, Massachusetts, Michigan, Minnesota, Missouri, New York, North Carolina, Ohio, Pennsylvania, Texas, Washington.
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-1291-2022 (June 2, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1291-2022 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.