Tornier Stryker Perform Reversed Glenoid Press-Fit Short Post: Incorrect Device in Package
Recall of Tornier Stryker Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V (REF DWJ001, L: 7mm) due to incorrect device in labeled package. Affected units include specific batch and serial numbers.
Lower-risk recall
The incorrect device is contained in the labeled package.
Contact the company
What happened, in plain English
Tornier is recalling a specific type of surgical implant because it was incorrectly packaged. This means the device might not be the right one for the patient, which could lead to complications during surgery. Read more at govinfonow.com/recall/56414-tornier-stryker-perform-reversed-glenoid-press-fit-short-post-incorrect.
Source Summary by GovInfoNow · govinfonow.com/recall/56414-tornier-stryker-perform-reversed-glenoid-press-fit-short-post-incorrect · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0773-2024
Cite this page
“Tornier Stryker Perform Reversed Glenoid Press-Fit Short Post: Incorrect Device in Package.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56414-tornier-stryker-perform-reversed-glenoid-press-fit-short-post-incorrect. Based on FDA recall #Z-0773-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0773-2024%22&limit=1).
Why it’s dangerous
The device is labeled incorrectly in the package, meaning it might not be the right surgical implant for the procedure. This could cause improper fitting or complications during surgery if used without verification.
Who’s affected
Surgical patients and healthcare providers who received the recalled implant. Those most at risk are patients undergoing orthopedic surgery with this specific implant.
How to tell if you have this one
Check for batch lot code 6714AZ and serial numbers 001 to 050 on the implant packaging. The GTIN number is 00846832091614.
- Brand
Tornier- Product
Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile- Category
Medical device
What to do — step by step
Check Package Details
Look for batch lot code 6714AZ and serial numbers 001 to 050 on the implant packaging.
Where it went and when
Where it was distributed
Distributed in 9 states, and outside the U.S.
FDA distribution: “Distribution was made to AR, AZ, CA, CO, CT, NC, OH, TN, and VA. There was no military/government distribution. Foreign distribution was made to Australia, France, and Italy.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Arkansas, California, Colorado, Connecticut, North Carolina, Ohio, Tennessee, Virginia.
Recall timeline
FDA published this recall 28 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-0773-2024 (January 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0773-2024 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.