FDA Device Intelligence
HomeOWENS & MINOR DISTRIBUTION, INC. › MediChoice

MediChoice

OWENS & MINOR DISTRIBUTION, INC. · Model GZ5003 · UDI-DI 10885632069697

NAB
10
510(k) clearances
271
Adverse events (6 deaths)
6
Recalls
575
Facilities

Description

Fluff Gauze Sponge Sterile 10/Tray 4 Inch X 4 Inch Small 16-Ply 100% Cotton Hypoallergenic Single Use Only Not Made With Natural Rubber Latex MediChoice Non-Acute Only

Recalls

DateFirmReason
2020-11-05Medline Industries IncRevMedX Trauma Dressing is being recalled due to package seal integrity.
2018-12-27Cardinal Health 200, LLCCurity All Purpose Sponges were not sterilized and distributed
2018-10-16ASO, LLCPotential that gauze pads may not be fully sterilized
2015-08-12Revmedx IncThe XGAUZE Trauma Dressing was recalled because the packages may acquire small tears or pinholes during shipping due to use of shipping containers that lacked adequate protective m
2012-05-14Hartmann USA, IncMicro holes were detected in the laminate of the sterile barrier system of sterilized Hartmann Econolux and Hartmann Sterilux gauze products
2012-05-14Hartmann USA, IncMicro holes were detected in the laminate of the sterile barrier system of sterilized Hartmann Econolux and Hartmann Sterilux gauze products

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.