Welch Allyn Inc Mortara recalls

Welch Allyn Inc Mortara has 16 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 13 Oct 2021. 1 is still ongoing. The most frequent reason is device malfunction.

Total recalls16since 2020

Last 12 months0reported

Class I00% of total

Ongoing1latest 13 Oct 2021

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0

Severity split

Class I 0 0%Class II 16 100%Class III 0 0%

Why welch allyn inc mortara is recalled

Device Malfunction1594%
Other Reasons16%

Product types

By year

2021531%
20201169%

Ongoing welch allyn inc mortara recalls

1 active

Reported	Class	Recall	Company	Reason	Where
13 Oct 2021Device	CLASS II	ELI, Burdick and McKesson brand 280 Resting recalledMcKesson	Welch Allyn Inc Mortara	Device Malfunction	Nationwide

All welch allyn inc mortara recalls, newest first

16 total

Reported	Class	Recall	Company	Reason	Where
13 Oct 2021Device	CLASS II	ELI, Burdick and McKesson brand 280 Resting recalledMcKesson	Welch Allyn Inc Mortara	Device Malfunction	Nationwide
28 Apr 2021Device	CLASS II	ELI 380 Electrocardiograph, with AM12M Acquisition Module accessory recalled	Welch Allyn Inc Mortara	Device Malfunction	Nationwide
28 Apr 2021Device	CLASS II	ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory recalled	Welch Allyn Inc Mortara	Device Malfunction	Nationwide
28 Apr 2021Device	CLASS II	AM12M Acquisition Module accessory recalled by Welch Allyn Inc Mortara	Welch Allyn Inc Mortara	Device Malfunction	Nationwide
28 Apr 2021Device	CLASS II	Surveyor S12/S19 Bedside Patient Monitor recalled	Welch Allyn Inc Mortara	Device Malfunction	Nationwide
16 Dec 2020Device	CLASS II	ELI 380 Electrocardiograph recalled by Welch Allyn, Inc/mortara	Welch Allyn Inc/Mortara	Other	Nationwide
6 May 2020Device	CLASS II	Pat Cbl 10wire Leadform XL Aha Snap recalled by Welch Allyn, Inc/mortara	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	S4 and patient cable for the S4 Wireless Telemeter recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	ELI PC. The ELI PC Service automatically converts resting recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Q-Stress/XScribe recalled by Welch Allyn, Inc/mortara	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Q-Tel. The Q-Tel RMS system is a computer-based cardiac recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	T12. Incorporates wireless electrocardiographic technology recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Replaceable lead set for the Wireless Acquisition Module recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Surveyor S12/S19 and patient cable recalled by Welch Allyn, Inc/mortara	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Lead diagnostic electrocardiograph under the following recalled	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide
6 May 2020Device	CLASS II	Pat Cbl 10wire Leadform XL Aha Snap recalled by Welch Allyn, Inc/mortara	Welch Allyn Inc/Mortara	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.