FDA Device Intelligence
Home › Leica Biosystems Richmond, Inc. › Leica Biosystems

Leica Biosystems

Leica Biosystems Richmond, Inc. · Model 39LC-550-11-L · UDI-DI 20849832003285

IDZ
5
510(k) clearances
48
Adverse events
1
Recalls
57
Facilities

Description

IP Routine VI Cassettes, Taped, Gray

Recalls

DateFirmReason
2013-04-04Leica Microsystems, Inc.An LPC Fine Mesh Cassette failed to stay closed during processing operations.

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.