Facility

Kayserbetten GmbH & Co. KG

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

Key facts

1recalls · worst Class I

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3006795806
Establishment type	Manufacture Medical Device
Location	Rieper Str. 12 Dorfmark Lower Saxony, DE 29683
Registration status	Active · expires 2026
Parent company	Kayserbetten GmbH & Co. KG (owner-operator 10023012)
Brand names	Timmy; Olaf,; IDA II (KR13); KayserBett Hannah135 (KR5); KayserBett Hannah170 (KR5); IDA I (KR3)

Activity by year

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…

All facilities operated by Kayserbetten GmbH & Co. KG

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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