ConMed recalls Mini Infant < 3kg Radiotranslucent Electrodes with adhesive on contact wires that may impede conductivity and cause device failure. Affected units include specific lot numbers.
Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
ConMed is recalling Mini Infant < 3kg radiotranslucent electrodes because adhesive on the contact wires may impede conductivity and cause device failure. This could lead to improper pacing or defibrillation in pediatric patients.
The adhesive on the contact wires may impede conductivity, which could lead to improper pacing or defibrillation. This is a potential failure in the device's ability to safely interface with the patient's skin.
Pediatric patients under 10 kg (22 lbs) using the Mini Infant electrodes. Parents and caregivers of infants with specific lot numbers are most at risk.
Check for the product name 'Mini Infant < 3kg Radiotranslucent Electrode' with the Physio-Control Quik-Combo connector. Affected units have specific lot numbers listed in the recall notice.
Look for the lot numbers listed in the recall notice: Y013114-14, Y04191607, Y061413-09, and other specific codes.
ConMed's Mini Infant < 3kg Radiotranslucent Electrode with Physio-Control Quik-Combo connector, REF/Catalog Number 2602M.
The adhesive on contact wires may impede conductivity, potentially causing device failure during pacing or defibrillation.
Check the lot number on the product; affected units include specific codes like Y013114-14, Y04191607, and others listed in the recall notice.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1177-2018 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-1177-2018 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.
