FDA Device Intelligence
HomeSTERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model J-0140 · UDI-DI 10885403191435

HAE Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities

Description

V. Mueller Neuro/Spine LEKSELL RONGEUR, REGULAR CURVE DOUBLE ACTION 2MM JAW OVERALL LENGTH 9-1/2 inches 24CM

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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.