Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1813-2020Class II

T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF...

Mortara Instrument, Inc. / initiated 2020-03-18 / Terminated / root cause: design

WELCH ALLYN, INC/MORTARA began a recall of T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF transmission of simultaneous 12-lead ECG data with... on . FDA classified it as Class II and gives the reason as "Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment". As of , the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number
Z-1813-2020
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Mortara Instrument, Inc.
Product
T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF transmission of simultaneous 12-lead ECG data with diagnostic quality while allowing the patient to be ambulatory.
Product code
DPS Electrocardiograph
Reason for recall
Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.
Root cause tag
design
FDA root cause
Device Design
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.
Quantity in commerce
78,521 units total
Distribution
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.
Product codes and lots
Model Numbers: T12-XXX-XXXXX, T12S-XXX-XXXXX.

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1813-2020
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1810-2020Class IITerminatedVoluntary: Firm initiated
Z-1811-2020Class IITerminatedVoluntary: Firm initiated
Z-1812-2020Class IITerminatedVoluntary: Firm initiated
Z-1813-2020Class IITerminatedVoluntary: Firm initiated
Z-1814-2020Class IITerminatedVoluntary: Firm initiated
Z-1815-2020Class IITerminatedVoluntary: Firm initiated
Z-1816-2020Class IITerminatedVoluntary: Firm initiated
Z-1817-2020Class IITerminatedVoluntary: Firm initiated
Z-1818-2020Class IITerminatedVoluntary: Firm initiated
Z-1819-2020Class IITerminatedVoluntary: Firm initiated