Leonhard Lang Medizintechnik recalls

Leonhard Lang Medizintechnik has 4 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 20 Sep 2017. The most frequent reason is sterility.

Total recalls4since 2015

Last 12 months0reported

Class I250% of total

Ongoing0latest 20 Sep 2017

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 2 50%Class II 2 50%Class III 0 0%

Why leonhard lang medizintechnik is recalled

Sterility250%
Device Malfunction250%

Product types

By year

2017125%
2016125%
2015250%

All leonhard lang medizintechnik recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
20 Sep 2017Device	CLASS I	Skintact Electrode for Defibrillation, Pacing, Monitoring recalled	Leonhard Lang Medizintechnik	Sterility	FL, TX
26 Oct 2016Device	CLASS I	Skintact Electrodes for Defibrillation, DF29N recalled	Leonhard Lang Medizintechnik	Sterility	FL
25 Nov 2015Device	CLASS II	ECG Electrodes: 50007 Stablebase SBW55 50675 Stablebase recalled	Leonhard Lang Medizintechnik	Device Malfunction	FL
8 Apr 2015Device	CLASS II	Skintact ECG Electrode FS recalled by Leonhard Lang Medizintechnik	Leonhard Lang Medizintechnik	Device Malfunction	FL

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.