Kayserbetten GmbH & Co. KG
1 recall(s) on record — most severe on record: Class I.
Recalls by year
- Recalls (1)
Registered facilities (1)
- Kayserbetten GmbH & Co. KG FEI 3006795806 · DE
Recalls & enforcement
- Class IOngoing2026-05-04If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased risk that the patient (child) or third parties (children) will operate the hand control and trap themse…
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. “Kayserbetten GmbH & Co. KG — 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-10023012-kayserbetten-gmbh-co-kg/
Alerts for Kayserbetten GmbH & Co. KG
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.