Encore Medical Recalls Turon Glenoid Reamer Due to Incorrect Spherical Radius
Encore Medical recalls specific Turon Glenoid Reamer models with incorrect spherical radius cutting surface that may cause improper bone cutting during surgery.
Lower-risk recall
It was reported that the models used to manufacture S-200956/958 had the wrong dimension used to create the spherical radius cutting surface. Device design allows a larger spherical radius cutting surface than intended.
Contact the company
What happened, in plain English
Encore Medical is recalling certain Turon Glenoid Reamers that have a manufacturing defect causing an incorrect spherical radius cutting surface. This could lead to improper bone cutting during surgical procedures if used as intended. Read more at govinfonow.com/recall/73250-encore-medical-recalls-turon-glenoid-reamer-due-to-incorrect-spherical.
Source Summary by GovInfoNow · govinfonow.com/recall/73250-encore-medical-recalls-turon-glenoid-reamer-due-to-incorrect-spherical · Updated September 19, 2026 · FDA enforcement record: FDA #Z-3102-2017
Cite this page
“Encore Medical Recalls Turon Glenoid Reamer Due to Incorrect Spherical Radius.” GovInfoNow, updated September 19, 2026. https://govinfonow.com/recall/73250-encore-medical-recalls-turon-glenoid-reamer-due-to-incorrect-spherical. Based on FDA recall #Z-3102-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3102-2017%22&limit=1).
Why it’s dangerous
The recalled devices have a larger spherical radius cutting surface than intended due to a manufacturing error. This could result in improper bone cutting during surgical procedures if the device is used as designed.
Who’s affected
Orthopedic surgeons and medical professionals who use the recalled Turon Glenoid Reamers for bone surgery are most at risk. Patients receiving these procedures may be affected if the device is used incorrectly.
How to tell if you have this one
Check for catalog numbers REF S-200956 (5mm PIN, SIZE 46), REF S-200957 (5mm PIN, SIZE 50), or REF S-200958 (5mm PIN, SIZE 58). The lot numbers for these models are 535U1000, 536U1000, and 537U1000 respectively.
- Brand
Encore Medical- Category
Medical device
What to do — step by step
Check Device Details
Verify the catalog number and lot number on the device to determine if it is recalled.
Where it went and when
Where it was distributed
Distributed in Ohio and Virginia.
FDA distribution: “OH, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio, Virginia.
Recall timeline
FDA terminated this recall 5.9 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-3102-2017 (August 4, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3102-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 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.