# FDA recall Z-2130-2024

> **ZOLL Medical Corporation** · Class I · device recall initiated 2024-04-30.

## Product

ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide and Quick Reference Guide (QRGs) as follows:    Part Numbers:	  1.	799-EGL2-02  2.	799-EGL2-02-01  3.	799-EGL2-02-04  4.	799-EGL2-02-05  5.	799-EGL2-02-08  6.	799-EGL2-02-10  7.	799-EGL2-02-11  8.	799-EGL2-02-15  9.	799-EGL2-02-16  10.	799-EMBP-05-01  11.	799-EMBP-05-02  12.	799-EMBP-05-08  13.	799-EMBP-05-10  14.	799-EMBP-05-11  15.	799-EMBP-05-12  16.	799-EMBP-05-12-68  17.	799-EMBP-05-16  18.	799-EMBP-05-23  19.	799-EMVP-05  20.	799-EMVP-05-01  21.	799-EMVP-05-05  22.	799-EMVP-05-10  23.	799-EMVP-05-15  24.	799-EMVP-05-16    Manual Part Numbers  906-0731-01;  9650-002365-01 (US);  906-0731-01-05 (CAN);  906-0731-01-10;  9650-0002363-01;  906-0731-01 (Commercial);  906-0731-03 (Military);  9650-0002363-01;  9650-0002363-05;  906-0731-01;  906-0731-01-05 (CAN);  906-0731-01-04;  906-0731-01-05;  906-0731-01-08;  906-0731-01-10;  906-0731-01-11;  906-0731-01-15;  906-0731-01-16;  9650-0002363-01; 

## Reason for recall

Operator's Guide & Quick Reference Guide (QRG) ZOLL 731 Ventilator for MRI Compatible Devices. Patient Safety Ventilator MRI information omitted from the manuals. Update to the instructions ensures safe distance from the MRI to ensure proper function of the ventilator and reduce the risk of delay in ventilator therapy

## Distribution

Worldwide distribution - US Nationwide and the countries of United Arab Emirates,  Argentina, Australia, Azerbaijan, Bangladesh, Belgium, Bahrain, Bolivia, Brazil, Canada,  Switzerland, China, Colombia, Czech Republic, Germany, Spain, Great Britain (UK), Greece, Guatemala, Guam, Hong Kong, Croatia, Hungary, Indonesia, Israel, India, Iraq,  Italy, Japan, South Korea, Lebanon, Myanmar, Mexico, Malaysia, Netherlands, New Zealand, Oman, Panama, Philippines, Pakistan, Poland, Puerto Rico, Portugal, Qatar,  Romania, Saudi Arabia, Singapore, Thailand, Turkey, Taiwan, Vietnam.

## Key facts

- **Recall number:** Z-2130-2024
- **Recalling firm:** ZOLL Medical Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-30
- **Report date:** 2024-06-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chelmsford, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2130-2024

## Citation

> AI Analytics. FDA recall Z-2130-2024. Retrieved 2026-09-07 from https://api.ai-analytics.org/recall/Z-2130-2024. Source: US FDA. Licensed CC0.

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