TriMed UOCP-S Plate: Incorrect Saw Guide Alignment Risk

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Recalling firmTriMed Inc.27533 Avenue Hopkins · Santa Clarita, CA 91355-3910

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✎ GovInfoNow plain-language explainer

What happened, in plain English

TriMed is recalling short UOCP-S ulnar osteotomy compression plates because the saw guide holes are on the wrong side of the plate. This could lead to improper alignment during surgery, potentially causing complications.

Why it’s dangerous

The saw guide holes are positioned incorrectly on the plate, which could cause improper alignment during surgery. This might lead to inaccurate bone cuts or complications during the procedure.

Who’s affected

Surgical patients and medical professionals who use the TriMed UOCP-S plates for ulna osteotomy procedures. Those with lot numbers 10003 or 10017 are most at risk.

How to tell if you have this one

Check for the model number UOCP-S on the plate. Affected units have lot numbers 10003 or 10017. The plate is non-sterile and used in ulna osteotomy procedures.

Brand
TriMed
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Plate Model
Look for the model number UOCP-S on the plate to confirm it is affected.
Contact Manufacturer
Reach out to TriMed Inc. for specific guidance on next steps.

✎ GovInfoNow

Questions people ask

Is this plate used for surgery?

Yes, the UOCP-S is non-sterile and intended for use in ulna osteotomy procedures.

What lot numbers are affected?

Lot numbers 10003 and 10017 are affected.

How does this hazard affect surgery?

The saw guide holes are on the wrong side of the plate, which could cause improper alignment during surgery.

Take action

Contact TriMed

We’ve drafted a message you can send TriMed to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2877-2018 — TriMed TriMed

Hello,

I own a TriMed that is covered by recall Z-2877-2018 from TriMed.

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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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-2877-2018 (April 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2877-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 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.

TriMed Inc. recalls Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the

Use caution until it’s fixed