# FDA recall Z-1877-2019

> **GE Healthcare, LLC** · Class III · device recall initiated 2019-05-10.

## Product

Replacement leadwires with grabber ends:  REF/Catalog Number	Description  2106388-005	Replacement ECG Leadwire, grabber, BRN V, AHA, 74 cm/ 29 in  2106388-101	Replacement ECG Leadwire, grabber, LL , AHA, 130 cm/ 51 in  2106388-103	Replacement ECG Leadwire, grabber, GRN RL,  AHA, 130 cm/ 2106388-107	Replacement ECG Leadwire, grabber, BLK N, IEC, 130 cm/ 51 in  2106392-004	Replacement ECG Leadwire, grabber, ORG V, AHA, 74 cm/ 29 in    The reusable ECG leadwire sets enable ECG monitoring with GE equipment requiring rectangular 11-pin ECG trunk cable. Use leadwire sets with ECG trunk cable or telemetry transmitter.

## Reason for recall

ECG trunk cables and leadwires may reduce the amount of energy reaching the patient during defibrillation, potentially limiting success of defibrillating the patients rhythm.

## Distribution

Worldwide Distribution: US (nationwide)  including Puerto Rico, and countries of: Australia, Austria, Azerbaijan, Bangladesh, Belarus, Belgium, Bermuda, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, Chile, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Germany, Greece, Guernsey, Honduras, Hong Kong, Hungary, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Kenya, Korea (Republic of), Kuwait, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malta, Mauritius, Mexico, Moldova, Morocco, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Palestine (state of), Panama, Poland, Qatar, Republic of Serbia, Romania, Russia, Saudia Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Tajikistan, Tanzania, Thailand, Trinidad and Tobago, Turkey, Uganda, Ukraine, United Arab Emirates, United Kingdom, Ur

## Key facts

- **Recall number:** Z-1877-2019
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-10
- **Report date:** 2019-07-03
- **Termination date:** 2024-05-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1877-2019

## Citation

> AI Analytics. FDA recall Z-1877-2019. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-1877-2019. Source: US FDA. Licensed CC0.

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