Home › Aesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model GB042R · UDI-DI 04038653068623

LYS LXH Prescription

510(k) clearances

1,274

Adverse events

Recalls

Facilities

Description

Crushing drum

Recalls

Date	Firm	Reason
2006-10-20	Medtronic Sofamor Danek USA Inc	Metal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use.

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 key Read 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.