FDA Device Intelligence
HomeUNITED METAL FABRICATORS, INC. › UMF Medical

UMF Medical

UNITED METAL FABRICATORS, INC. · Model 4070-650-100B · UDI-DI 00815235020439

INQ
10
510(k) clearances
47
Adverse events (2 deaths)
2
Recalls
53
Facilities

Description

4070-650 HI-LO POWER EXAM TABLE - STANDARD- BASE ONLY

Recalls

DateFirmReason
2016-06-29ARJOHUNTLEIGH POLSKA Sp. z.o.o.ArjoHuntleigh has concluded that a device tipping hazard may occur on the current Sara Combilizer lifting mechanism, providing a potential for risk to the patient or the caregiver.
2009-01-26Phillips Nuclear MedicineA problem has been identified with some upper patient pallets on Precedence SPECT/CT System, which may reduce its load bearing capacity and may result in its cracking. If this were

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.