FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model AU5464 · UDI-DI 10885403008191

KCP Prescription
4
510(k) clearances
26
Adverse events
1
Recalls
143
Facilities

Description

V. Mueller REINER EAR SYRINGE 4 OZ 120CC CAPACITY WITH SHIELD and 2 TIPS, STRAIGHT and BULBOUS

Recalls

DateFirmReason
2003-04-30Medegen Medical Products, LLCFinished products were not sterilized.

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.