Device Recall Henora

Model / Serial
Lot numbers 102131 and 110531.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
US Nationwide Distribution in the states of AL, CA, DE, GA, IL, KY, MA, MD, ME, MI, MN, NJ, NM, NV, NY, OH, TN, TX, WA, and WI.
Product Description
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set || Product Usage: || Catheter extension set for high pressure procedures.
Manufacturer
RGI Medical Manufacturing, Inc.
1 Event
- Recall of Device Recall Henora

Manufacturer

RGI Medical Manufacturing, Inc.

Manufacturer Address
RGI Medical Manufacturing, Inc., 4637 NW 6th St, Gainesville FL 32609-0701
Manufacturer Parent Company (2017)
Rgi Medical Manufacturing Inc.
Source
USFDA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)