Home › CROSSTEX INTERNATIONAL, INC. › Ultra Gauze Non-Woven Sponges
Ultra Gauze Non-Woven Sponges
CROSSTEX INTERNATIONAL, INC. · Model ENCNWU · UDI-DI 10732224001071
10
510(k) clearances
271
Adverse events (6 deaths)
6
Recalls
575
Facilities
Description
Non-Woven, 4 Ply, Non-Sterile, 2" x 2"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-05 | Medline Industries Inc | RevMedX Trauma Dressing is being recalled due to package seal integrity. |
| 2018-12-27 | Cardinal Health 200, LLC | Curity All Purpose Sponges were not sterilized and distributed |
| 2018-10-16 | ASO, LLC | Potential that gauze pads may not be fully sterilized |
| 2015-08-12 | Revmedx Inc | The 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 |
| 2012-05-14 | Hartmann USA, Inc | Micro holes were detected in the laminate of the sterile barrier system of sterilized Hartmann Econolux and Hartmann Sterilux gauze products |
| 2012-05-14 | Hartmann USA, Inc | Micro 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 docsData 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.