RegWardenFDA facility compliance records
Facility

Kayserbetten GmbH & Co. KG

1 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2026: 1 recalls20172018201920202021202220232024202512026
  • Recalls (1)

Devices registered here (1)

  • Bed, Ac-Powered Adjustable Hospital
    Product code FNL (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5100

Recalls & enforcement

  • Class IOngoing2026-05-04
    If 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…

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Kayserbetten GmbH & Co. KG (FEI 3006795806) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006795806-kayserbetten-gmbh-co-kg/

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