Overview of recall records associated with Leonhard Lang Gmbh, including dates, categories and classifications where available.
Classification mix: Class I: 1.
The firm discovered that during the use of these defibrillation electrodes a possibility for arcing and a resulting malfunction exists. This could lead to a situation, in which a patient…
This page summarizes recall records in which the official source identifies Leonhard Lang Gmbh as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
