Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI 280, ELI 380, R-Scribe and Connex Cardio. Product Usage: A non-invasive prescription device indicated for use to acquire, analyze, display, transmit and print electrocardiograms.
FDA Recall Z-1810-2020 · Posted 2020-04-29
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Recalling FirmWELCH ALLYN, INC/MORTARA
Recall StatusTerminated
Product CodeDPS
Date Initiated2020-03-18
Date Terminated2026-02-09
Product Quantity78,521 units total
Reason for Recall
Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.
Firm Action
Welch Allyn notified customers on 2/19/2020 via "Voluntary Medical Device Correction Welch Allyn Patient Cables or Lead Sets". The recall letter identified the affected product and stated the reason for the recall. The firm also requested the distributors to immediately notify accounts if the product was further distributed.
Root Cause
Device Design
Distribution Pattern
US nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, ON, OR, PA, PR, RI, SC, SD, TN,UT, VA, VT, WA, WI, WV and WY.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
K102206ELI 10 ELECTROCARDIOGRAPH MODEL ELI 10Mortara Instrument, Inc. · 2011-02-18K101403ELI 250 ELECTROCARDIOGRAPHMortara Instrument, Inc. · 2010-07-02K101115ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150Mortara Instrument, Inc. · 2010-06-18K100127ELI 230 ELECTROCARDIOGRAPHMortara Instrument, Inc. · 2010-04-16K092663ELI 350 ELECTROCARDIOGRAPHMortara Instrument, Inc. · 2009-12-14
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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