Olymp: Always-On Tip Tracked Instruments (SPiN Drive) Forceps with model INS-0362 may have EM sensor tracking issues causing navigation errors during endobronchial procedures, potentially delaying surgery. Affected units include specific lot numbers.
Electromagnetic (EM) sensor tracking malfunction impacts the use of navigation functionality during endobronchial procedures and prompts the system to report a coil break warning message. This could result in a potential procedural delay
Olympus is recalling SPiN Drive Forceps (model INS-0362) due to electromagnetic sensor tracking problems that could cause navigation errors during endobronchial procedures, potentially delaying surgery. This recall affects specific lot numbers and models sold for clinical use.
The EM sensor tracking system may malfunction during navigation, prompting a 'coil break' warning message. This could lead to procedural delays but does not indicate immediate safety risks like injury or death.
Healthcare professionals using these forceps during endobronchial procedures are most at risk. The recall applies to specific lot numbers and models sold for clinical interventions.
Check for model number INS-0362 and lot numbers 05010210512 and below on the instrument packaging. These forceps are intended for clinical use in endobronchial procedures.
Look for model number INS-0362 on the instrument packaging.
Confirm lot numbers 05010210512 and below to determine if the instrument is affected.
The EM sensor tracking system may malfunction during navigation, prompting a 'coil break' warning message, which could cause procedural delays.
Check the model number (INS-0362) and lot number (05010210512 and below) to see if it's affected. If so, contact Olympus for further instructions.
The recall indicates a potential for procedural delays but does not mention injury risks. The hazard is described as not causing immediate safety concerns.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2263-2023 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2263-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
