FDA Device Intelligence
HomeUNITED PRODUCTS & INSTRUMENTS › UNICO

UNICO

UNITED PRODUCTS & INSTRUMENTS · Model CMH30 · UDI-DI 00816668020003

GKG
10
510(k) clearances
30
Adverse events
4
Recalls
18
Facilities

Description

CMH30 Microhematocrit Centrifuge, 24 place rotor, 5 minute timer. 110V

Recalls

DateFirmReason
2009-11-21Hettich Instruments Management ICentrifuge Rotor Failure: may crack, break, and explode outside the centrifuge.
2009-11-21Hettich Instruments Management ICentrifuge Rotor Failure: may crack, break, and explode outside the centrifuge.
2009-11-21Hettich Instruments Management ICentrifuge Rotor Failure: may crack, break, and explode outside the centrifuge.
2009-11-21Hettich Instruments Management ICentrifuge Rotor Failure: may crack, break, and explode outside the centrifuge.

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.