Data Foundry

Medical device recalls 2018

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart… — Class II medical device recall Z-2737-2018

Terminated recall by Natus Neurology DBA Excel Tech., Ltd. (XLTEK), reported 2018-08-15, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Natus Neuro has discovered a possible manufacturing defect in the ErgoJust mobile cart that may cause the cart

Recall numberZ-2737-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNatus Neurology DBA Excel Tech., Ltd. (XLTEK), Oakville, N/A, Canada
Recall initiated2018-05-18
Classified2018-08-08
Reported by FDA2018-08-15
Terminated2020-08-04
DistributedAK, 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
Countries outside the USAT, CA, CH, CO, CR, CZ, DE, FR, HK, IL, JO, JP, KR, LV, MY, OM, PH, PT, RS, SA, SI
Quantity797 total
Model numbers021240

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2737-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.