FDA Device Intelligence
HomeHU-FRIEDY MFG. CO., LLC › HU-FRIEDY

HU-FRIEDY

HU-FRIEDY MFG. CO., LLC · Model ASPB2 · UDI-DI 10889950004354

EHZ
10
510(k) clearances
9
Adverse events
1
Recalls
141
Facilities

Description

B2 Byrd Self-Cleaning Aspirator

Recalls

DateFirmReason
2022-11-02Stradis Medical, LLC dba Stradis HealthcareMedical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in

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.