# FDA recall Z-2737-2018

> **Natus Neurology DBA Excel Tech., Ltd. (XLTEK)** · Class II · device recall initiated 2018-05-18.

## Product

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video Extension, EuroJust ICU Cart Export For PTZ Video Ext.     Video cart used for mobile medical record documentation.

## Reason for recall

Natus Neuro has discovered a possible manufacturing defect in the ErgoJust mobile cart that may cause the cart s video pole to fail.

## Distribution

United States Distribution:  AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV.    Worldwide Distribution: Austria, Canada, Colombia, Costa Rica, Czech Republic, France, Germany, Hong Kong, Israel, Japan, Jordan, Korea, ,Republic of Latvia, Malaysia, Oman, Philippines, Portugal, Saudi Arabia, Serbia, Slovenia, Switzerland.                                                                                                                                                                                                                                                                                                                                                                                                            Sold To Location State  AK  AL  AR  AZ  CA  CO  CT  DC  DE  FL  GA  IA  ID  IL  IN  KS  KY  LA  MA  MD  MI  MN  MO  MS  MT  NC  ND  NE  NH  NJ 

## Key facts

- **Recall number:** Z-2737-2018
- **Recalling firm:** Natus Neurology DBA Excel Tech., Ltd. (XLTEK)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-18
- **Report date:** 2018-08-15
- **Termination date:** 2020-08-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oakville, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2737-2018

## Citation

> AI Analytics. FDA recall Z-2737-2018. Retrieved 2026-06-29 from https://api.ai-analytics.org/recall/Z-2737-2018. Source: US FDA. Licensed CC0.

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