Northgate Technologies recalls ACMI 9FR probes (NTI Catalog 72-00198-0) due to failed biocompatibility testing. This may pose health risks during medical procedures.
Investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.
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.
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.
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.
Check for the NTI catalog number 72-00198-0 on the probe packaging. These probes are used for urinary/renal and biliary procedures.
Look for the NTI catalog number 72-00198-0 on the probe packaging.
The probes failed biocompatibility testing, which could pose health risks during medical procedures.
The recall record does not specify a remedy, so contact Northgate Technologies for guidance.
The recall indicates the probes failed biocompatibility testing, so they are not safe for use.
We’ve drafted a message you can send Northgate Technologies to request your refund or repair — edit it as you like.
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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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.
