Physio-Control recalls infant/child reduced energy defibrillation electrodes (part number 3202380-006) for use with LIFEPAK 1000, 500, and CR Plus/EXPRESS defibrillators due to improperly sealed packaging. This could lead to contamination or damage.
Packaging of infant child reduced energy electrodes was not properly sealed.
Physio-Control is recalling infant and child reduced energy defibrillation electrodes that were manufactured between August 2017 and October 2019. The packaging was not properly sealed, which could lead to contamination or damage of the electrodes.
The packaging was not properly sealed, which could allow contaminants to enter the electrodes. This might cause damage to the electrodes or affect their performance during use.
Healthcare professionals and emergency responders who use the LIFEPAK 1000, 500, or CR Plus/EXPRESS defibrillators with the recalled electrodes. Those who are not trained in emergency medical response may not be affected.
Look for the part number 3202380-006 on the packaging. The electrodes were manufactured between August 2017 and October 2019 and have not expired.
Inspect the packaging for proper sealing. If the packaging is not sealed, do not use the electrodes.
The packaging of the infant and child reduced energy defibrillation electrodes was not properly sealed, which could lead to contamination or damage.
The part number is 3202380-006.
The electrodes were manufactured between August 2017 and October 2019.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-2359-2020 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-2359-2020 from Physio-Control. 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.