VOLT Wrist Treatment System: Incorrect Thread Orientation Recall

Take action

Contact the company & request your remedy

Recalling firmTyber Medical83 S Commerce Way Ste 310 · Bethlehem, PA 18017-8934

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

VOLT's left wrist treatment plates have incorrect thread orientation. This could lead to improper fitting and potential injury during use. Affected models are identifiable by their specific model number and size.

Why it’s dangerous

The plates have incorrect thread orientation, which may cause improper fitting. This could lead to complications during surgery or treatment if the device doesn't align correctly with the bone structure.

Who’s affected

Users of VOLT's left wrist treatment plates with model number 02.426.691S (186mm) are most at risk. This affects medical professionals and patients using the device for wrist treatment.

How to tell if you have this one

Check for model number 02.426.691S on the plate. The product is a left anatomical plate measuring 186mm. It was manufactured in lot 291293.

Brand
VOLT
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Number
Look for model number 02.426.691S on the plate to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The supplier manufactured anatomical left plates with an incorrect thread orientation, which may cause improper fitting.

How can I tell if I have the recalled product?

Check for model number 02.426.691S on the plate. The product is a left anatomical plate measuring 186mm.

What should I do if I have the recalled product?

The recall record does not specify a remedy, so contact VOLT directly for guidance.

Take action

Contact VOLT

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

✉️ Open in email

Subject: Recall Z-1132-2026 — VOLT VOLT

Hello,

I own a VOLT that is covered by recall Z-1132-2026 from VOLT.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1132-2026 (December 19, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1132-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

Tyber Medical recalls Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm

Lower-risk recall