Exactech recalls reverse shoulder humeral liners with articular surface outside dimensional specs. Affected models include 320-38-00, 320-38-03, 320-42-00, and 320-42-03 with specific UDI numbers. Contact for remedy.
Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
Exactech is recalling reverse shoulder humeral liners that have an articular surface position outside the labeled dimensional specifications. This could lead to improper joint alignment and potential complications during surgery.
The articular surface of the humeral liners may be positioned outside the dimensional specifications stated in the product labeling. This could cause improper joint alignment during surgery, potentially leading to complications.
Patients who received these specific humeral liners during surgery are likely affected. Surgeons and medical teams using the recalled models are at the highest risk.
Check for the model numbers 320-38-00, 320-38-03, 320-42-00, or 320-42-03 with the corresponding UDI numbers listed in the recall notice.
Reach out to Exactech directly to confirm if your specific humeral liner model is affected and to receive guidance on next steps.
The recall indicates the articular surface may be outside dimensional specifications, so they are not safe for use as intended.
Contact Exactech directly to confirm if your specific model is affected and to receive guidance on next steps.
Check for the model numbers 320-38-00, 320-38-03, 320-42-00, or 320-42-03 with the corresponding UDI numbers listed in the recall notice.
We’ve drafted a message you can send Exactech to request your refund or repair — edit it as you like.
Subject: Recall Z-2561-2025 — Exactech Exactech Hello, I own a Exactech that is covered by recall Z-2561-2025 from Exactech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
