Civco recalls VirtuTRAX Instrument Navigator sensors with specific lot numbers due to potential failure to tighten onto instruments. Affected units may not function properly during medical procedures.
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Civco is recalling Virtu:TRAX Instrument Navigators with certain lot numbers because they might not tighten securely onto medical instruments. This could lead to improper use during procedures if the device becomes loose.
The device may not tighten properly onto medical instruments, which could cause it to become loose during use. This might lead to improper function or failure to stay securely attached during medical procedures.
Medical professionals using the VirtuTRAX device with the listed lot numbers are most at risk. Patients using these devices during procedures may also be affected if the device fails to stay securely attached.
Check the lot numbers on the device: A117795, A119539, A121993, A129844, A131074, A131075, A131690, or A142178. The product includes a specific part number (5350925) and UDI (00841436100892).
Look for the lot numbers listed: A117795, A119539, A121993, A129844, A131074, A131075, A131690, or A142178.
The device may not tighten securely onto medical instruments, which could cause it to become loose during use.
Check the lot numbers on the device: A117795, A119539, A121993, A129844, A131074, A131075, A131690, or A142178.
The recall does not specify a remedy, so contact Civco Medical Instruments Co. Inc. for further instructions.
We’ve drafted a message you can send Civco Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0395-2022 — Civco Medical Civco Medical Hello, I own a Civco Medical that is covered by recall Z-0395-2022 from Civco Medical. 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.
