LEONHARD LANG GMBH
1 recall(s) on record — most severe on record: Class I.
Recalls by year
- Recalls (1)
Registered facilities (1)
- LEONHARD LANG GMBH FEI 6736 · AT
Recalls & enforcement
- Class ITerminated2014-12-03The 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 who is in a life threatening situation requiring a defibrillation can receive such therapy o…
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “LEONHARD LANG GMBH — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-8020045-leonhard-lang-gmbh/
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