Olympus CD-B62: Mispackaged Hemostasis Probe Risk

Take action

Contact the company & request your remedy

Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy, N/A · Center Valley, PA 18034-8229

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling Hemostasis Probes model CD-B622LA because they were mispackaged and labeled incorrectly as having a fixed pin connector when they actually have a coaxial plug. This mislabeling could lead to improper use if someone assumes the probe has a fixed pin connector.

Why it’s dangerous

The probe was mislabeled as having a fixed pin connector when it actually has a coaxial plug. This could cause improper connections if someone assumes it has a fixed pin connector, potentially leading to incorrect use in medical procedures.

Who’s affected

Healthcare professionals using the Hemostasis Probe model CD-B622LA are likely affected. Those who have the specific model number and lot number from the recall list are at risk of using the wrong connector type.

How to tell if you have this one

Check for the model number CD-B622LA and lot number KR214212 on the probe. The product was sold with specific UDI/DI: 00821925039452.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model and Lot Number
Look for model number CD-B622LA and lot number KR214212 on the probe.

✎ GovInfoNow

Questions people ask

Why is this probe being recalled?

The probe was mispackaged and labeled as having a fixed pin connector when it actually has a coaxial plug.

What should I do if I have this probe?

Check the model number and lot number to see if it matches the recalled units. If it does, contact Olympus for guidance.

Is there a fix for this issue?

The recall record does not mention a remedy or fix.

Take action

Contact Olympus

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

✉️ Open in email

Subject: Recall Z-1481-2024 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1481-2024 from Olympus.

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-1481-2024 (January 5, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1481-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Olympus Corporation of the Americas recalls Hemostasis Probe, Model: CD-B622LA

Lower-risk recall