# FDA device recall: Pediatric care bed;  Product Designation: KayserBett IDA;

> recall · VERIFIED · 2026-05-04

Firm: KAYSERBETTEN GMBH & CO. KG · Class I · 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 (

- Company: KAYSERBETTEN GMBH & CO. KG
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.