Physio-Control recalls LIFEPAK Electrode Starter Kits with incorrect infant pad placement instructions and missing safety symbols. Consumers should check product details to avoid improper use during emergencies.
The infant artwork on the product instructs incorrect pad placement. Also, the artwork is missing the Type BF Patient connection and High Voltage Warning symbols.
Physio-Control is recalling LIFEPAK Electrode Starter Kits because the infant artwork shows incorrect pad placement and lacks critical safety symbols. This could lead to improper use during emergencies if someone tries to apply the pads without following the correct instructions.
The product includes artwork that shows incorrect pad placement for infants, which could lead to improper use during emergencies. Additionally, the missing Type BF Patient connection and High Voltage Warning symbols increase the risk of accidental injury if the device is used incorrectly.
Parents or caregivers who use these electrode kits for infants or children are most at risk. The recall affects users who follow the incorrect pad placement instructions on the product.
Check for the product catalog number 11101-000017 and minimum serial number 3202784-009. These kits are sold with LIFEPAK EXPRESS, CR Plus, 1000, or 500 Biphasic AEDs that have a pink connector.
Look for the catalog number 11101-000017 and minimum serial number 3202784-009 on the kit packaging.
The recall is happening because the infant artwork shows incorrect pad placement and the product is missing critical safety symbols like Type BF Patient connection and High Voltage Warning.
No, but you should check the product details to ensure you have the recalled version. The hazard does not require immediate stop-use, but proper use is important for safety.
The official recall notice does not specify a remedy, so you should check the product details and contact Physio-Control for further guidance.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-0187-2018 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-0187-2018 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.
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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.
