FDA Device Intelligence
Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model FF141 · UDI-DI 04038653065196

HBM Prescription
3
510(k) clearances
94
Adverse events
2
Recalls
32
Facilities

Description

CASPAR HEAD CUSHION F/HEAD SUPPORT

Recalls

DateFirmReason
2023-12-12Steris CorporationDual-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.
2023-12-12Steris CorporationDual-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 docs
Data 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.