Home › Black Forest Medical GmbH › DORO® Adaptor
DORO® Adaptor
Black Forest Medical GmbH · Model 3011-00 · UDI-DI 04250435501375
HBM
Prescription
3
510(k) clearances
94
Adverse events
2
Recalls
32
Facilities
Description
DORO® Side Rail Adaptor
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-12 | Steris Corporation | Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay. |
| 2023-12-12 | Steris Corporation | Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.