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Leonhard Lang Medizintechnik GmbH recalls

Every recall we track for Leonhard Lang Medizintechnik GmbH — 1 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

1recalls

Recalls per year, by danger level

1 recall since 2017.

2017: 1 recall — 1 use caution120172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 0 recalls20212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Leonhard Lang Medizintechnik GmbH 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.

Recalls per year for Leonhard Lang Medizintechnik GmbH, by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201701001
201800000
201900000
202000000
202100000
202200000
202300000
202400000
202500000
2026 (to date)00000

What to do if you have a recalled Leonhard Lang Medizintechnik GmbH product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Leonhard Lang Medizintechnik GmbH recalls

1 shown

Leonhard Lang Medizintechnik GmbH recall questions

How many recalls has Leonhard Lang Medizintechnik GmbH had?

1 recall from Leonhard Lang Medizintechnik GmbH are on record with U.S. safety agencies, from 2017.

What is the most recent Leonhard Lang Medizintechnik GmbH recall?

Leonhard Lang Medizintechnik GmbH recalls Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for, dated Aug 8, 2017. Every Leonhard Lang Medizintechnik GmbH recall is listed on this page, newest first.

What should I do if I have a recalled Leonhard Lang Medizintechnik GmbH 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 Leonhard Lang Medizintechnik GmbH 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.