Pediatric care bed — Class I medical device recall Z-2212-2026
Ongoing recall by KAYSERBETTEN GMBH & CO. KG, reported 2026-06-10, distributed nationwide. If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided
| Recall number | Z-2212-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | KAYSERBETTEN GMBH & CO. KG, Bad Fallingbostel, Germany |
| Recall initiated | 2026-05-04 |
| Classified | 2026-06-04 |
| Reported by FDA | 2026-06-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 372 units |
| Serial numbers | 10350, 10351, 10352, 1072, 1073, 1074, 1075, 1076, 1077, 1078, 1079, 1080, 1081, 10819, 1082, 10820, 10821, 10822, 10823, 10824, 10825, 1083, 1085, 1086, 1087 and 347 more |
Product
Pediatric care bed; Product Designation: KayserBett IDA;
Reason for recall
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 themselves or others under the bed frame or between the bed frame and the floor. This can lead to serious injuries or even death of the patient (child) or third parties (children).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2212-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.