ConMed recalls Electrosurgical Suction Coagulators 10FR with potential suction port occlusion, risking procedure delays. Affected units have specific lot codes and catalog numbers.
Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
ConMed is recalling certain Electrosurgical Suction Coagulators that may have suction ports that become blocked. This could delay surgery and require using another device, which is risky during procedures.
Suction ports may become blocked during use, preventing the device from functioning properly. This could delay surgery and force the use of another device, which might not be available or suitable in critical situations.
Surgical teams using the affected models are most at risk. Patients undergoing procedures with these devices could face delays or need alternative equipment.
Check for the catalog number 130187 and lot codes 202204294 through 202208084. The device is a foot-controlled electrosurgical suction coagulator sold under ConMed.
Verify if your device has the catalog number 130187 and one of the listed lot codes.
Suction ports may become blocked, preventing the device from functioning during surgery and potentially causing delays or requiring another device.
Check if your device has the catalog number 130187 and one of the listed lot codes. If so, contact ConMed for further instructions.
The recall states the device may cause procedure delays and require another device, but does not mention injury risks. The hazard is not severe enough for immediate stop-use.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-0474-2023 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-0474-2023 from ConMed. 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.
