# FDA recall Z-0187-2018

> **Physio-Control, Inc.** · Class I · device recall initiated 2017-10-27.

## Product

LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009     The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.

## Reason for recall

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.

## Distribution

Worldwide distribution: US (nationwide) including Puerto Rico and Guam and countries of: Canada, Austria, Belgium, Czech Republic; Denmark, Finland, France, French Polynesia, Germany, Hungary, Ireland, Italy, Latvia, Netherlands, Australia, China, Hong Kong, Japan, Argentina, Mexico, Norway, Panama,  Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom, and New Zealand.

## Key facts

- **Recall number:** Z-0187-2018
- **Recalling firm:** Physio-Control, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-27
- **Report date:** 2017-12-20
- **Termination date:** 2019-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Redmond, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0187-2018

## Citation

> AI Analytics. FDA recall Z-0187-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0187-2018. Source: US FDA. Licensed CC0.

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