T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF...
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| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-1810-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1811-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1812-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1813-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1814-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1815-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1816-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1817-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1818-2020 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1819-2020 | Class II | Terminated | Voluntary: Firm initiated |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
