DJO Surgical RSP Glenoid Baseplate Recall: Coating Hex Won't Engage With Tools
DJO Surgical recalls RSP Glenoid Baseplate model 508-32-204 due to coating hex not engaging with standard tools, risking improper installation.
Use caution until it’s fixed
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
Contact the company
What happened, in plain English
DJO Surgical is recalling a specific shoulder surgery implant because its coating hex won't properly engage with standard tools, which could lead to improper installation during surgery. Read more at govinfonow.com/recall/57364-djo-surgical-rsp-glenoid-baseplate-recall-coating-hex-won-t.
Source Summary by GovInfoNow · govinfonow.com/recall/57364-djo-surgical-rsp-glenoid-baseplate-recall-coating-hex-won-t · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0532-2024
Cite this page
“DJO Surgical RSP Glenoid Baseplate Recall: Coating Hex Won't Engage With Tools.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/57364-djo-surgical-rsp-glenoid-baseplate-recall-coating-hex-won-t. Based on FDA recall #Z-0532-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0532-2024%22&limit=1).
Why it’s dangerous
The coating hex on the baseplate doesn't properly engage with standard hex drivers or screwdrivers. This can cause improper installation during surgery, potentially leading to complications.
Who’s affected
Surgical teams using the RSP Glenoid Baseplate model 508-32-204 for shoulder procedures are affected. Surgeons and surgical technicians who have this implant are most at risk.
How to tell if you have this one
Check for the model number 508-32-204 on the product. The serial numbers 769P2825, 769P2846, and 769P2893 are also associated with this recall.
- Brand
DJO Surgical- Category
Medical device
What to do — step by step
Check Product Details
Verify the model number and serial numbers listed in the recall notice to confirm if your device is affected.
Where it went and when
Where it was distributed
Distributed in 17 states and Puerto Rico.
FDA distribution: “U.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX, VA, and WA O.U.S.: None” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Florida, Indiana, Kansas, Kentucky, Maine, Minnesota, Mississippi, New Jersey, Ohio, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Washington.
Recall timeline
FDA published this recall 3 months 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-0532-2024 (September 6, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0532-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.