Northgate ACMI 9FR Probe Recall: Biocompatibility Test Failure

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Recalling firmNorthgate Technologies, Inc.1591 Scottsdale Ct, N/A · Elgin, IL 60123-9361

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Northgate Technologies recalls AC:MI 9FR probes (NTI catalog number 72-00198-0) because they failed biocompatibility testing. This could cause health issues during medical procedures.

Why it’s dangerous

The probes failed biocompatibility testing, meaning they may not be safe for contact with human tissue. This could lead to health issues during medical procedures if used improperly.

Who’s affected

Medical professionals using these probes for urinary/renal or biliary procedures are likely affected. Patients undergoing such procedures with these probes may be at risk.

How to tell if you have this one

Check for the NTI catalog number 72-00198-0 on the probe packaging. These probes are used for urinary/renal and biliary procedures.

Brand
Northgate Technologies
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the NTI catalog number 72-00198-0 on the probe packaging.

✎ GovInfoNow

Questions people ask

Why is this probe being recalled?

The probes failed biocompatibility testing, which could pose health risks during medical procedures.

What should I do if I have this probe?

The recall record does not specify a remedy, so contact Northgate Technologies for guidance.

Is this probe safe for use?

The recall indicates the probes failed biocompatibility testing, so they are not safe for use.

Take action

Contact Northgate Technologies

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

✉️ Open in email

Subject: Recall Z-1885-2020 — Northgate Technologies Northgate Technologies

Hello,

I own a Northgate Technologies that is covered by recall Z-1885-2020 from Northgate Technologies.

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-1885-2020 (March 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1885-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Northgate Technologies, Inc. recalls ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies, America (OSTA); NTI Catalog Number 72-00198-0 -

Recall notice