Welch Allyn Inc Mortara recalls
Every recall we track for Welch Allyn Inc Mortara — 16 in all, from 2020–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Welch Allyn Inc Mortara peaked in 2020 (11); 16 since 2017.
All FDA recall records for Welch Allyn Inc Mortara since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 2 | 7 | 11 |
| 2021 | 0 | 0 | 3 | 2 | 5 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Welch Allyn Inc Mortara recalls
What to do if you have a recalled Welch Allyn Inc Mortara product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Welch Allyn Inc Mortara recalls
4 shown- UnratedMedical device
Welch Allyn Inc Mortara recalls ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers:
Welch Allyn recalls ELI 280 Resting Electrocardiographs with specific model numbers and software versions due to malfunction under certain operator workflows. No remedy stated in official notice.
Welch Allyn Inc MortaraSep 3, 2021 - Lower riskMedical device
Welch Allyn Inc Mortara recalls Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the
Welch Allyn recalls Surveyor S12/S19 bedside patient monitors with AM12M acquisition module software version 1.5.1 that do not meet IEC 60601-2-27 safety standards. Affected units have specific serial numbers and part numbers listed in the recall notice.
Welch AllynMar 31, 2021 - Lower riskMedical device
WELCH ALLYN, INC/MORTARA recalls ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.
Welch Allyn recalls ELI 380 electrocardiographs due to potential wireless disconnection from access points, which may disrupt medical monitoring. Affected units have specific part numbers listed in the recall notice.
Welch AllynNov 11, 2020 - UnratedMedical device
WELCH ALLYN, INC/MORTARA recalls X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL
Welch Allyn recalls X12+ Telemeter patient cables that may not meet defibrillation safety standards. Affected units could pose a risk during medical use. Contact Welch Allyn for details.
Welch AllynMar 18, 2020
Welch Allyn Inc Mortara recall questions
How many recalls has Welch Allyn Inc Mortara had?
16 recalls from Welch Allyn Inc Mortara are on record with U.S. safety agencies, from 2020–2021.
What is the most recent Welch Allyn Inc Mortara recall?
Welch Allyn Inc Mortara recalls ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers:, dated Sep 3, 2021. Every Welch Allyn Inc Mortara recall is listed on this page, newest first.
Why are Welch Allyn Inc Mortara products recalled?
The most common reasons on record: Devices do not meet IEC 60601-2-27 requirements as labeled. (4).
What should I do if I have a recalled Welch Allyn Inc Mortara product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Welch Allyn Inc Mortara recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.